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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384194Generated: November 2, 2026

Pyridine → Isobutyl (3-methoxy-5-methylpyrazin-2-yl)carbamate

https://huagongshe.com/reaction/1384194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIsobutyl chloroformateHCID 62365—
Reactant3-Methoxy-5-methyl-2-pyrazinamineHCID 10701894—
SolventDichloromethaneHCID 6344—
ProductIsobutyl (3-methoxy-5-methylpyrazin-2-yl)carbamateHCID 10889995—

Reaction Steps

Isobutylchloroformate (4.79 ml) was added to a stirred solution of 2-amino-3-methoxy-5-methylpyrazine (5 g) and pyridine (2.91 ml) in dichloromethane (10 ml) at ambient temperature. After 90 minutes the reaction mixture was diluted with dichloromethane (10 ml) and washed with 2M hydrochloric acid (3×20 ml), water (20 ml) and saturated sodium chloride solution (20 ml) and then dried (MgSO4). Volatile material was removed by evaporation to give a solid which was recrystallised from hexane to give isobutyl N-(3-methoxy-5-methylpyrazin-2-yl)carbamate (6.5 g); 1H NMR (CDCl3): 1.0 (d, 6H), 2.0 (m, 1H), 2.4 (s, 3H), 4.0 (d, 2H), 4.02 (s, 3H), 7.3 (s, 1H), 7.8 (s, 1H); mass spectrum (postive chemical ionisation (+ve CI)): 240 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258817B1
Source datasetuspto-grants-2001_07
ORD IDord-77bcb29d30d842be96d2e9c2a46af28a
Source noteuspto-grants-2001_07