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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605099Generated: October 30, 2026

3-Methoxyaniline → HCID 67040482, compound

https://huagongshe.com/reaction/605099

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyanilineHCID 10824—
ReactantHCID 86615545HCID 86615545—
ProductHCID 67040482HCID 67040482—

Reaction Steps

A solution of the product from Example 43D and 3-Methoxy-phenylamine was reacted to provide 4-(4-Benzyloxy-phenoxy)-3-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-N-(3-methoxy-phenyl)-benzamide using the procedure from Example 43E. The material was then deprotected using the procedure from Example 43F to provide the crude title compound which was purified by column chromatography on silica gel using methanol/dichloromethane as eluent to provide the title product (12 mg, 40%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.32 (d, J=6.99 Hz, 6 H) 3.11-3.29 (m, 1 H) 3.75 (s, 3 H) 6.68 (dd, J=8.09, 1.84 Hz, 1 H) 6.75 (d, J=8.82 Hz, 2 H) 6.89 (t, J=8.64 Hz, 3 H) 7.24 (t, J=8.09 Hz, 1 H) 7.37 (d, J=8.09 Hz, 1 H) 7.45 (t, J=2.21 Hz, 1 H) 7.60 (d, J=8.46 Hz, 1 H) 7.86 (dd, J=8.64, 1.65 Hz, 1 H) 8.17 (s, 1 H) 8.61 (s, 1 H) 8.82 (d, J=8.46 Hz, 1 H) 9.38 (s, 1 H) 10.01 (s, 1 H) 10.15 (s, 1 H); MS (ESI+) m/z 522 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910595B2
Source datasetuspto-grants-2011_03
ORD IDord-740bcd982920452e9e3a2062da0b7ffa
Source noteuspto-grants-2011_03