Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607235Generated: October 30, 2026

2-(4-Fluoro-phenylsulfanyl)-5-methyl-phenylamine → (7-Cyclopropyl-pyrido[2,3-d]pyrimidin-4-yl)-[2-(4-fluoro-phenylsulfanyl)-5-methyl-phenyl]-amine

https://huagongshe.com/reaction/607235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Fluoro-phenylsulfanyl)-5-methyl-phenylamineHCID 43168932—
Reactant4-(2-Amino-4-methyl-phenylsulfanyl)-phenolHCID 66808123—
ReactantN'-(3-Cyano-6-cyclopropyl-pyridin-2-yl)-N,N-dimethyl-formamidineHCID 66808412—
ReactantN'-(3-Cyano-6-methyl-pyridin-2-yl)-N,N-dimethyl-formamidineHCID 66808573—
Product(7-Cyclopropyl-pyrido[2,3-d]pyrimidin-4-yl)-[2-(4-fluoro-phenylsulfanyl)-5-methyl-phenyl]-amineHCID 66808336—

Reaction Steps

2-(4-Fluoro-phenylsulfanyl)-5-methyl-phenylamine was reacted with the product from Example 119A using the procedure from Example 102 substituting 2-(4-Fluoro-phenylsulfanyl)-5-methyl-phenylamine for the product from Example 6c and substituting the product from Example 119A for the product from Example 10B to provide the crude residue which was purified by trituration with methanol to provide the title compound. 1H NMR (300 MHz, DMSO-D6) δ ppm: 0.96-1.19 (m, J=6.25 Hz, 4H), 2.22-2.42 (m, 1H), 2.33 (s, 3H), 7.02-7.28 (m, 6H), 7.33 (s, 1H), 7.56 (d, J=8.46 Hz, 1H), 8.46 (s, 1H), 8.66 (d, J=8.09 Hz, 1H), 10.03 (s, 1H); MS (ESI)+ m/z 403 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-e75693b6c8a04afcbb09a25ff9c180f4
Source noteuspto-grants-2011_03