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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947509Generated: October 26, 2026

Acetic Anhydride → 4-(Acetyl-cyclopropyl-amino)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1947509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 4-(cyclopropylamino)piperidine-1-carboxylateHCID 2769591—
SolventDichloromethaneHCID 6344—
Product4-(Acetyl-cyclopropyl-amino)-piperidine-1-carboxylic acid tert-butyl esterHCID 68772516—

Reaction Steps

To a solution of 4-cyclopropylamino-piperidine-1-carboxylic acid tert-butyl ester (1.0 g, 4.2 mmol) in DCM (22 mL) was added DIEA (0.8 mL, 4.6 mmol) and acetic anhydride (0.42 mL, 4.4 mmol). The mixture was stirred (rt, 16 h). After washing the solution with 1 N NaOH and brine, the organic layer was dried and concentrated to an orange oil (1.15 g, 98%). MS (ESI): mass calcd. for C15H26N2O3, 282.19; m/z found, 283.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399465B2
Source datasetuspto-grants-2013_03
ORD IDord-9b7014b6dd8341e88cd311bec1b2a3b3
Source noteuspto-grants-2013_03