Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278311Generated: October 31, 2026

HCID 11296511, compound → HCID 11399167, compound

https://huagongshe.com/reaction/278311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11296511HCID 11296511—
SolventSodium HydroxideHCID 14798—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 11399167HCID 11399167—

Reaction Steps

1-(4-Bromo-benzyl)-4-[4-(4-morpholin-4-yl-but-2-ynyloxy)-benzenesulfonyl]-piperidine-4-carboxylic acid was prepared starting from 1-(4-bromo-benzyl)-4-[4-(4-morpholin-4-yl-but-2-ynyloxy)-benzenesulfonyl]-piperidine-4-carboxylic acid ethyl ester (2.87 g, 4.6 mmol) dissolved in THF:methanol (3:1, 150 ml) and 10 N NaOH (10 ml). The resulting reaction mixture was worked up as outlined in Example 1 (Step 7). Yield 2.26 g (83%); white powder; mp 198° C.; MS: 593.1 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358980B1
Source datasetuspto-grants-2002_03
ORD IDord-0e34ba198fd2460b8576e297b85e51b0
Source noteuspto-grants-2002_03