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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607195Generated: October 30, 2026

N'-(3-Cyano-pyridin-2-yl)-N,N-dimethyl-formamidine → 4-[4-(4-Methoxy-benzyloxy)-2-(pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenol

https://huagongshe.com/reaction/607195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'-(3-Cyano-pyridin-2-yl)-N,N-dimethyl-formamidineHCID 66808319—
Reactant4-[2-Amino-4-(4-methoxy-benzyloxy)-phenylsulfanyl]-phenolHCID 66808407—
Reactant4-[2-Amino-4-(3-fluoro-benzyloxy)-phenylsulfanyl]-phenolHCID 66808677—
Product4-[4-(4-Methoxy-benzyloxy)-2-(pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenolHCID 6680834555%

Reaction Steps

The product from Example 10E and the product from Example 57A were reacted according to the procedure in Example 57E substituting the product of Example 10E for the product of Example 57D to provide a solid which was triturated with methanol to provide the title compound (49 mg, 55%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 10.07 (s, 1H), 9.63 (s, 1H), 9.05 (s, 1H), 8.83 (s, 1H), 8.58 (s, 1H), 7.64 (s, 1H), 7.38 (d, J=8.46 Hz, 2H), 7.20-7.29 (m, 1H), 7.12-7.18 (m, 1H), 7.06-7.12 (m, 2H), 6.90-6.99 (m, 3H), 6.62-6.69 (m, 2H), 5.02 (s, 2H), 3.75 (s, 3H); MS (ESI+) m/z 483.2 (M+H)+, (ESI−) m/z 481.2 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-f9d1b567f0f64fcfb5b75bbfb913cf9b
Source noteuspto-grants-2011_03