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www.tractuschem.com
Tractus
Presentation
Tractus Company Limited
Unit5, 3/F Harry Industrial Building
4951 Au Pui Wan Street, Fo Tan
Shatin, New Territories
Hong Kong
Tel: +852 8198 2399
Email: contact@tractuschem.com
website: www.tractuschem.com
www.tractuschem.com
TractusAbout Us
To dedicate ourselves to generating exceptional values through providing high quality and
cost-effective products and services for the benefit of our customers and the community.
Our Mission
US educated management team with combined 30 years experience in pharmaceutical industry;
Scientists including Ph.D. chemists from top Chinese universities and institutions.
Our People
Modern research and development laboratory.
Massive production facility
Our Facility
Custom process research and development;
Custom synthesis from milligrams to tens of kgs;
Custom manufacture of APIs and key intermediates to hundreds of tons;
Custom analytical development.
Our Services
Products and services at competitive prices;
Technical abilities;
Your Benefits
www.tractuschem.com
Tractus
Chem/Pharma Products
Building Blocks *
Lab Reagents *
Active Pharmaceutical Ingredients (APIs)
Integrated Services
Analytical Service *
Sourcing / Logistics Service *
Drug Discovery Support Service
Process Research and Development Service
Contract Research/Manufacturing Service
FTE Program
Core Business
www.tractuschem.com
TractusLocation
Nanjing
Shanghai
Hong Kong
Nanjing Chemical Industry Park
(One of only two government owned Chemical Industry Parks)
19 miles from downtown Nanjing
36 miles from Nanjing International Airport
Area
2548 sq. miles
Population
6.24 million
Geographic
Nanjing
190 miles from
Shanghai
750 miles from Beijing
Tractus R&D and Production
Chemical Industry Park
Zijin Mountain
Nanjing
Downtown
Nanjing Yangtse River
Second Bridge
www.tractuschem.com
Tractus
PROJECT
MANAGEMENT TEAM
Direct
Communication
Weekly
Update
Campaign
Report
Feasibility
Study
Lab
Optimization
Kilo Lab
Pilot
Plant
Full-scale
Production
Customer
Enquiry
Secrecy
Agreement
Evaluation/
Quotation
Project
Preparation
Project
Execution
Project
Completion
PROJECT
TECHNICAL TEAM
Project Management
www.tractuschem.com
Tractus
Total Area :
50 Acr es
11.5 Acres for
future development
Site Plot
www.tractuschem.com
TractusR&D and Kilo Lab
Ph.D. chemists: 4
MS chemists: 11
BS chemists: 34
Technicians: 2
20,000 sq. ft. modern laboratory
55 fume hoods including 8 walking hoods
GC and HPLC system
20 Foot walk-in fume hoods
20L, 30L and 50L jacketed glass reactors
20L and 50L rotary evaporators
Temperature range from -78℃ to 200℃
2L and 5L high pressure stainless steel
hydrogenator
Associated addition and work up equipments
Overview
www.tractuschem.com
TractusAnalytical Equipments
300 MHz Bruker NMR 1
Agilent LC/MS 1
Shimadzu GC/MS 2010 1
Agilent HPLC 10
Shimadzu HPLC 2
Shimadzu GC 2010 4
Overview
www.tractuschem.com
Tractus
Pilot Plants: 3
1000 L Glass-lined Reactors: 3
500 L Glass-lined Reactors: 8
300 L Glass-lined Reactors: 4
200 L Glass-lined Reactors: 6
100 L Glass-lined Reactors: 10
50 L Glass-lined Reactors: 20
Centrifuges: 6
Warm-Wind Cycle Ovens: 5
Vacuum Dryers: 6
High Pressure Hydrogenation Plant: 1
2000L SS316 High Pressure Reactors (Up to 11MPa): 2
1000L SS316 Glass-lined Reactor (Up to 1.6MPa): 1
Overview
Pilot Plant
www.tractuschem.com
TractusProduction-Capacity
Raw Materials: 22,600 sq. foot
Finished Products: 93,000 sq. foot
Reactors:
500 L to 3000 L Glass-lined reactors
500 L to 3000 L SS316 reactors
-20℃ - 200℃
Up to 50 bar
Purified water system
Steam
Cooling water system
Waste treatment facility
Vertical in SS304, SS316
Driers Mills
Temperature:
Pressure:
Supporting Systems:
Centrifuges:
Warehouse:
www.tractuschem.com
TractusProduction
www.tractuschem.com
TractusQC/QA
Qualified Analysts: 12
Validated Analytical Methods
Qualified Instruments
10 HPLC’s
4 GC’s
1 FT-IR and 1 UV-Vis
4 Stability Chambers
1 Bio Lab
Qualified QA Specialists: 10
Quality System: GMP/ICH
Overview
www.tractuschem.com
TractusNew R&D Center
www.tractuschem.com
Tractus
Besides our FTE and customer synthesis services, we have a group of R&D chemists
dedicated to the development of in-house technologies and new product lines.
Chiral amino acid synthesis using Scholkopt bislactim.
Chiral building blocks using chiral amino acid and reduction technology.
In-House Technology
www.tractuschem.com
TractusCase Study- Darapladib
Darapladib
N
N
O
S
N
O
NH3C
H3C
CF3
F
Product Name: Darapladib
CAS#: 356057-34-6
Purity: >99%(HPLC, area)
Mol. W 666.77
www.tractuschem.com
Tractus
Br
CHO
F3C
B
OH
OH
+
Pd(OAc)2 (3%aq.)
Na2CO3/H2O/DME
OHC CF3
H3C N
NH2
H3C
2 3 4
5
1)
2) NaBH4/EtOH/THF
reflux 2h
73%
/toluene, rt. 48h
84%
CF3
H
N
NH3C
H3C
Biphenyl aldehyde 4 was prepared in 73% yield by Suzuki coupling of 4-trifluoromethylbenzeneboronic acid 2
and 4-bromobenzaldehyde 3. The conversion of 4 to diamine 5 was achieved in 84% yield by reductive
amination with N,N-diethylethylenediamine. Diamine 5 was used in the next step without further purification.
Darapladib
Case Study- Darapladib
www.tractuschem.com
Tractus
N
N
O
S
N
O
NH3C
H3C
CF3
F
O
O
EtO
+
NH2
NH2
S
DBU/CH3CN HN
N
O
HS
6 7 8
HN
N
O
S
F
9
Cl
F
K2CO3/acetone
N
N
O
S
F
O
O
N
N
O
S
F
OH
O
CF3COOH/DCM
Br
O
O
cat.KI/K2CO3/DMF
10 11
5
i-PrNEt, TBTU/DCM
Darapladib
70-80¡æ
20h
64%
reflux 4h
90%
0¡æ, 2h
87%
rt. 24h
95%
CF3
H
N
NH3C
H3C
rt. 16h
60% 1
Case Study- Darapladib
Darapladib
www.tractuschem.com
Tractus
Thiouracil 8 was synthesized in 64% yield by the condensation of ethyl 2-oxocyclopentanecarboxylate 6 and
thiourea 7. Thiouracil 8 was alkylated with 4-fluorobenzyl chloride to give 9 in 90% yield, which reacted with tert-
butyl bromoacetate to furnish adduct 10 in 87% yield. Cleavage of tert-butyl ester was achieved by treating with
trifluoroacetic acid, and product 11 was obtained in 95% yield in >98% purity after crystallization from EtOH.
Coupling of diamine 5 and carboxylic acid 11 in the presence of HBTU [94790-37-1], followed by crystallization
from isopropyl acetate gave Darapladib 1 in 60% yield and >99% purity.
Darapladib 1 exists in 1HNMR as a mixture of rotamers in about 1.2:1 ratio; and that ratio was 1.9:1 in literature.
1H-NMR and ESI-MS are consistent to its structure. The melting point of 125-126oC is identical to the report of
125oC.
Darapladib
Case Study- Darapladib
www.tractuschem.com
TractusScholkopt Bislactim
N
N
MeO
OMe
N
N
MeO
OMe
We developed practical synthesis of both reagents, for
Complexed chiral amino acid synthesis.
Both reagents are available in kg quantities with good
Chemical and chiral purity.
www.tractuschem.com
TractusScholkopt Bislactim for Chiral Amino Acid Synthesis
N
N
MeO
OMe
n-BuLi
F
F
F
Br
N
N
OMe
OMe F
F
F
F
F
F
NH2
N
O
N
N
N
CF3
Merck’s Medicinal synthesis of stigliptin.
Reference: J. Med. Chem. 2005, 141.
www.tractuschem.com
TractusScholkopt Bislactim for Chiral Amino Acid Synthesis
O OMe
OMe
Br
N
N
OMe
MeO
MeO
OMeO
N
N
OMe
MeO
nBuLi
MeO
OMeO
i-Pr
i-Pr
OH
H
N
O
MeMe
NH2
O
I-Pr
H2N
i-Pr
Reference: Helv. Chim. Acta. 2003, 2848.
www.tractuschem.com
Contact Us
Hong Kong office:
Unit5, 3/F Harry Industrial Building
4951 Au Pui Wan Street, Fo Tan
Shatin, New Territories
Hong Kong
Email: contact@tractuschem.com
website: www.tractuschem.com

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