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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754954Generated: October 29, 2026

1-Piperidinecarbonyl chloride → HCID 66815991, compound

https://huagongshe.com/reaction/1754954

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Piperidinecarbonyl chlorideHCID 242085—
ReactantHCID 66817168HCID 66817168—
SolventDichloromethaneHCID 6344—
ProductHCID 66815991HCID 6681599115.1%

Reaction Steps

TEA (1.143 mmol, 3 eq) and piperidine-1-carbonyl chloride (0.457 mmol, 1.2 eq) were sequentially added to a mixed solution of 8-(3-chloro-benzenesulfonyl)-2-piperidin-3-yl-1,3,8-triaza-spiro[4.5]dec-1-en-4-one trifluoroacetate (200 mg, 0.38 mmol) in dichloromethane (3 ml). The resulting mixture was stirred at room temperature overnight and then concentrated under reduced pressure. The resulting residue was purified by HPLC to give 8-(3-chloro-benzenesulfonyl)-2-[1-(piperidine-1-carbonyl)-piperidin-3-yl]-1,3,8-triaza-spiro[4.5]dec-1-en-4-one (30 mg, yield 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-9d348206c816410e84973a6680ee7be8
Source noteuspto-grants-2015_10