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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605104Generated: October 31, 2026

Anthranilamide → HCID 67040389, compound

https://huagongshe.com/reaction/605104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilamideHCID 6942—
ReactantHCID 86615545HCID 86615545—
ProductHCID 67040389HCID 67040389—

Reaction Steps

A solution of the product from Example 43D and 2-Amino-benzamide was reacted to provide 4-(4-Benzyloxy-phenoxy)-N-(2-carbamoyl-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 (18 mg, 34%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.35 (d, J=6.99 Hz, 6 H) 3.28 (m, 1 H) 6.76 (m, 2 H) 6.96 (m, 3 H) 7.18 (m, 1 H) 7.57 (m, 1 H) 7.85 (m, 4 H) 8.10 (d, J=2.21 Hz, 1 H) 8.43 (s, 1 H) 8.68 (d, J=8.46 Hz, 1 H) 8.91 (s, 1 H) 9.00 (d, J=8.82 Hz, 1 H) 9.48 (s, 1 H) 11.50 (s, 1 H) 12.99 (s, 1 H); MS (ESI+) m/z 535 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910595B2
Source datasetuspto-grants-2011_03
ORD IDord-96dcc2c3e8e14912b87e982f8d14c27d
Source noteuspto-grants-2011_03