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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607196Generated: October 30, 2026

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

https://huagongshe.com/reaction/607196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'-(3-Cyano-pyridin-2-yl)-N,N-dimethyl-formamidineHCID 66808319—
Reactant4-[2-Amino-4-(2-methoxy-benzyloxy)-phenylsulfanyl]-phenolHCID 66808543—
Reactant4-[2-Amino-4-(3-fluoro-benzyloxy)-phenylsulfanyl]-phenolHCID 66808677—
Product4-[4-(2-Methoxy-benzyloxy)-2-(pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenolHCID 6680842656%

Reaction Steps

The product of Example 37A was reacted with the product of Example 57A using the procedure of Example 57E substituting the product of Example 37A for the product of Example 57D to provide a solid which was triturated with methanol to provide the title compound (47 mg, 56%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 10.08 (s, 1H), 9.63 (s, 1H), 9.07 (s, 1H), 8.85 (d, J=6.62 Hz, 1H), 8.59 (s, 1H), 7.64 (s, 1H), 7.41 (dd, J=7.35, 1.47 Hz, 1H), 7.30-7.38 (m, 1H), 7.24 (s, 1H), 7.16 (d, J=8.46 Hz, 1H), 7.08-7.14 (m, 2H), 7.05 (d, J=8.09 Hz, 1H), 6.89-7.01 (m, J=7.54, 7.54 Hz, 2H), 6.61-6.71 (m, 2H), 5.05 (s, 2H), 3.80 (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-4594a11e3d5b427384103d29cf0436c7
Source noteuspto-grants-2011_03