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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401576Generated: November 1, 2026

Triethylamine → HCID 66873110, compound

https://huagongshe.com/reaction/2401576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 45139441HCID 45139441—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66873110HCID 6687311035.1%

Reaction Steps

To absolution of 4-aminomethyl-4-tert-butoxycarbonylamino-piperidine-1-carboxylic acid tert-butyl ester (12.2 mg, 0.037 mmol) and triethylamine (16 μL, 0.12 mmol) in dry dichloromethane (4 mL) was added 4-chlorobenzoyl chloride (5 μL, 0.037 mmol). After stirring for 18 hours at room temperature, the reaction mixture was partionated between dichloromethane (2 mL) and water (1 mL) with 10% aqueous sodium hydroxide (0.1 mL). The two layers were separated and the aqueous phase was further extracted with dichloromethane (2 mL). The combined organic layers were dried (Mg2SO4), filtered and concentrated. Preparative TLC, eluting with 10% methanol-dichloromethane, gave 4-tert-butoxycarbonylamino-4-[(4-chloro-benzoylamino)-methyl]-piperidine-1-carboxylic acid tert-butyl ester (6 mg, 0.013 mmol, 35%). LC-MS (LCT2) m/z 490 [M+Na+], Rt 8.20 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796293B2
Source datasetuspto-grants-2014_08
ORD IDord-dc1e4446e06b4b82935ab959218dc935
Source noteuspto-grants-2014_08