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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281671Generated: October 31, 2026

Triethylamine → HCID 86682348, compound

https://huagongshe.com/reaction/2281671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactanttert-butyl 1,6-diazaspiro[3.3]heptane-6-carboxylate, hemioxalate saltHCID 56962145—
SolventDichloromethaneHCID 6344—
ProductHCID 86682348HCID 86682348177.9%

Reaction Steps

To a stirred solution of 6-(tert-butoxycarbonyl)-1,6-diaza-spiro[3.3]heptane oxalate (350 mg, 719 μmol) in dichloromethane (6 mL) was added at 0° C. triethylamine (221 μl, 1.58 mmol) followed by 4-fluorobenzene-1-sulfonyl chloride (294 mg, 1.51 mmol). The reaction mixture was stirred at ambient temperature for 15 h. Further 4-fluorobenzene-1-sulfonyl chloride (100 mg, 0.51 mmol) and triethylamine (200 μl, 1.4 mmol) were added, the reaction mixture was stirred at ambient temperature for another 3 h. The reaction mixture was then diluted with dichloromethane 10 mL) and quenched with water (10 mL). The aqueous phase was extracted with CH2Cl2, and the combined organic phases were washed with brine, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by chromatography (SiO2; heptane:ethyl acetate 2:1) to give the title compound (456 mg, 89%) as a colorless oil. MS (EI) m/e: 357.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139593B2
Source datasetuspto-grants-2015_09
ORD IDord-9c196789ee114bce966a9c460fa3730a
Source noteuspto-grants-2015_09