5-Methyl-2-phenylsulfanyl-phenylamine → 7-cyclopropyl-N-(5-methyl-2-phenylsulfanyl-phenyl)pyrido[2,3-d]pyrimidin-4-amine

Participants

Role	Name	HCID	Charge
Reactant	5-Methyl-2-phenylsulfanyl-phenylamine	HCID 43349603	—
Reactant	4-(2-Amino-4-methyl-phenylsulfanyl)-phenol	HCID 66808123	—
Reactant	N'-(3-Cyano-6-cyclopropyl-pyridin-2-yl)-N,N-dimethyl-formamidine	HCID 66808412	—
Reactant	N'-(3-Cyano-6-methyl-pyridin-2-yl)-N,N-dimethyl-formamidine	HCID 66808573	—
Product	7-cyclopropyl-N-(5-methyl-2-phenylsulfanyl-phenyl)pyrido[2,3-d]pyrimidin-4-amine	HCID 57391392	—

Reaction Steps

The product from Example 5I was reacted with the product from Example 119A using the procedure from Example 102 substituting the product from Example 5I 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: 1.05-1.19 (m, 4H), 2.22-2.41 (m, 1H), 2.35 (s, 3H), 7.05-7.31 (m, 7H), 7.37 (s, 1H), 7.58 (d, J=8.46 Hz, 1H), 8.50 (s, 1H), 8.65 (d, J=8.46 Hz, 1H), 10.21 (s, 1H); MS (ESI)+ m/z 385 (M+H)+.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US07915411B2
Source dataset	uspto-grants-2011_03
ORD ID	ord-757a14f4b7814fefb6976e59612990e9
Source note	uspto-grants-2011_03