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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353544Generated: October 29, 2026

HCID 23513780, compound → HCID 23513915, compound

https://huagongshe.com/reaction/353544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23513780HCID 23513780—
ReactantHCID 86757881HCID 86757881—
ProductHCID 23513915HCID 2351391543%

Reaction Steps

Starting from 3-{[4-(2-butynyloxy)phenyl]sulfonyl}-1-(4-chlorobenzyl)-3-piperidinecarboxylic acid (1.1 g, 2.4 mmol) and and following the procedure as outlined in example 1, (step 8), 0.48 g of 3-{[4-(2-butynyloxy)phenyl]sulfonyl}-1-(4-chlorobenzyl)-3-N-hydroxy-3-piperidinecarboxamide hydrogen chloride was isolated as a white solid. Yield 43%; mp 124.4° C.; MS (ES): m/z: 477.1 (M+H)+; 1H NMR (300 MHz, DMSO-d6): δ2.0 (m, 2H), 3.39 (m, 5H), 4.27 (d, 2H), 4.89 (m, 2H), 7.14 (d, 2H), 7.15 (m, 4H), 7.61 (d, 2H), 8.95 (s, 1H), 9.46 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753337B2
Source datasetuspto-grants-2004_06
ORD IDord-48db68a1647645649a3bf245dae86b19
Source noteuspto-grants-2004_06