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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605101Generated: October 31, 2026

3-Aminopyridine → HCID 67040304, compound

https://huagongshe.com/reaction/605101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
ReactantHCID 86615545HCID 86615545—
ProductHCID 67040304HCID 67040304—

Reaction Steps

A solution of the product from Example 43D and Pyridin-3-ylamine was reacted to provide 4-(4-Benzyloxy-phenoxy)-3-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-N-pyridin-3-yl-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 (23 mg, 47%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.35 (d, J=6.99 Hz, 6 H) 3.29 (m, 1 H) 6.78 (m, 2 H) 6.95 (m, 3 H) 7.54 (dd, J=8.27, 4.96 Hz, 1 H) 7.90 (d, J=8.82 Hz, 1 H) 8.02 (dd, J=8.82, 2.21 Hz, 1 H) 8.16 (d, J=2.21 Hz, 1 H) 8.29 (m, 1 H) 8.39 (dd, J=4.78, 1.47 Hz, 1 H) 8.94 (s, 1 H) 9.04 (m, 2 H) 9.48 (s, 1 H) 10.59 (s, 1 H) 11.59 (s, 1 H); MS (ESI+) m/z 493 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910595B2
Source datasetuspto-grants-2011_03
ORD IDord-ffce4589daa24f59b2f41441a09ef49e
Source noteuspto-grants-2011_03