Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14868Generated: October 29, 2026

HCID 58603398, compound → HCID 58603532, compound

https://huagongshe.com/reaction/14868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58603398HCID 58603398—
Reactant4-{[5-(2-Chloro-pyrimidin-4-yl)-2-methoxy-benzyl]-methanesulfonyl-amino}-piperidine-1-carboxylic acid tert-butyl esterHCID 86603292—
ProductHCID 58603532HCID 58603532—

Reaction Steps

(N-(5-{2-[2-(3-Fluoro-4-hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-2-methoxy-benzyl)-N-piperidin-4-yl-methanesulfonamide: Intermediate 88 was coupled with intermediate 83 following procedure F. The resulting product was deprotected following procedure G. The product was purified by HPLC. LC-MS showed the product had the expected M+H+ of 530. 1H NMR (Varian 300 MHz, DMSO, shifts relative to the solvent peak at 2.50 ppm) δ 7.9 (d, 1H), 7.0 (m, 2H), 7.0 (m, 3H), 6.8 (m, 2H), 4.3 (s, 2H), 3.9 (s, 3H), 3.5 (d, 2H), 3.0 (s, 3H), 2.7 (m, 6H), 2.6 (m, 1H), 1.7-1.5 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732444B2
Source datasetuspto-grants-2010_06
ORD IDord-ce81976b59a440a8a9928f90fcdec50c
Source noteuspto-grants-2010_06