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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605107Generated: October 31, 2026

2-Bromoaniline → HCID 67040276, compound

https://huagongshe.com/reaction/605107

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanilineHCID 11992—
ReactantHCID 86615545HCID 86615545—
ProductHCID 67040276HCID 67040276—

Reaction Steps

A solution of the product from Example 43D and 2-Bromo-phenylamine was reacted to provide 4-(4-Benzyloxy-phenoxy)-N-(2-bromo-phenyl)-3-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-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 HPLC with TFA to provide the title compound as a trifluoroacetic acid salt (8 mg, 14%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.34 (d, J=6.99 Hz, 6 H) 3.28 (m, 1 H) 6.77 (m, 2 H) 6.94 (m, 3 H) 7.24 (m, 1 H) 7.44 (m, 1 H) 7.54 (dd, J=7.74, 1.84 Hz, 1 H) 7.73 (dd, J=8.09, 1.50 Hz, 1 H) 7.86 (d, J=8.46 Hz, 1 H) 8.01 (dd, J=8.64, 2.02 Hz, 1 H) 8.15 (d, J=2.21 Hz, 1 H) 8.89 (s, 1 H) 8.98 (d, J=8.46 Hz, 1 H) 9.46 (s, 1 H) 10.06 (s, 1 H) 11.37 (s, 1 H); MS (ESI+) m/z 570, 572 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910595B2
Source datasetuspto-grants-2011_03
ORD IDord-a145a25721c14c7793f006a37af9cc65
Source noteuspto-grants-2011_03