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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507308Generated: October 25, 2026

Trifluoroacetic acid → HCID 59001103, compound

https://huagongshe.com/reaction/507308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-{[N-((1R)-1-Carbamoyl-3-methyl-butyl)-N-(4-chlorobenzenesulfonyl)amino]-methyl}-piperidine-1-carboxylic acid tert-butyl esterHCID 59001095—
SolventDichloromethaneHCID 6344—
ProductHCID 59001103HCID 5900110384%

Reaction Steps

To a solution of 4-{[N-((1R)-1-carbamoyl-3-methyl-butyl)-N-(4-chlorobenzenesulfonyl)amino]-methyl}-piperidine-1-carboxylic acid tert-butyl ester (Example 92, 2.6 grams, 5.2 mmol) in CH2Cl2 (25 mL) was added trifluoroacetic acid (10 mL). The reaction was stirred at rt for 1 h and then was concentrated to give a white solid (1.6 grams, 84%). MS (ESI), (M+H)+ 402.15; 1H NMR (DMSO-d6, 500 MHz), δ 7-87 (d, 2H, J=8.5), 7.66 (d, 2H, J=8.6), 7.41 (s, 1H), 7.04 (s, 1H), 4.17 (t, 1H, J=7.3), 3.40-3.50 (m, 1H), 3.20-3.25 (m, 1H), 3.03-3.10 (m, 1H), 2.65-2.80 (m, 2H), 1.85-2.00 (m, 1H), 1.20-1.85 (m, 2H), 1.45-1.60 (m, 1H), 1.30-1.40 (m, 1H), 1.10-1.30 (m, 4H), 0.75-0.90 (m, 1H), 0.82 (d, 3H, J=7.3), 0.80 (d, 3H, J=7.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786122B2
Source datasetuspto-grants-2010_08
ORD IDord-6e03558616ed4e69bbac0b81b50fee9b
Source noteuspto-grants-2010_08