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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059893Generated: October 31, 2026

Water → Tert-butyl (1-(4-methylpyridin-2-yl)pyrrolidin-3-yl)carbamate

https://huagongshe.com/reaction/1059893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-methylpyridineHCID 2737403—
Reactanttert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
SolventDimethylformamideHCID 6228—
ProductTert-butyl (1-(4-methylpyridin-2-yl)pyrrolidin-3-yl)carbamateHCID 1866760754.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 2-fluoro-4-methylpyridine (1.11 g), 3-(tert-butoxycarbonylamino)pyrrolidine (1.68 g) and potassium carbonate (1.49 g) in N,N-dimethylformamide (20 ml) was stirred at 100° C. for 16 hours. After cooling, the mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water five times and brine, dried over sodium sulfate and evaporated under reduced pressure to give 1-(4-methylpyridin-2-yl)-3-(tert-butoxycarbonylamino)pyrrolidine (1.36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-9762b506dcbf498abef31fa08e845d4f
Source noteuspto-grants-2003_02