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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280663Generated: October 31, 2026

Sodium borohydride → N-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)ethyl]acetamide

https://huagongshe.com/reaction/1280663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantethyl (2RS)-2-acetylamino-3-(2-pyrazinyl)propanoateHCID 86584440—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)ethyl]acetamideHCID 22747907157.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

2.8 g of sodium borohydride are added to a solution of 8.5 g of ethyl (2RS)-2-acetylamino-3-(2-pyrazinyl)propanoate in 100 cm3 of ethanol and the mixture is then stirred at a temperature in the region of 20° C. After 18 hours, the reaction medium is taken up in 50 cm3 of water and 100 cm3 of dichloromethane and the aqueous phase is concentrated under reduced pressure (1 kPa) at a temperature in the region of 40° C. 11 g of N-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)-ethyl]acetamide are obtained in the form of a brown paste [1H NMR spectrum (300 MHz, (CD3)2SO-d6 with addition of a few drops of CD3COOD-d4 δ in ppm): 1.71 (s: 3H); 2.81 (dd, J=14.5 and 9 Hz: 1H); 3.03 (dd, J=14.5 and 5 Hz: 1H); 3.35 (dd, J=11 and 6 Hz); 3.42 (dd, J=11 and 5 Hz: 1H); 4.11 (mt: 1H); 7.75 (residual d, J=8.5 Hz: 0.5H); 8.45 (d, J=2.5 Hz: 1H); 8.50 (broad s: 1H); 8.53 (mt: 1H)]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451821B1
Source datasetuspto-grants-2002_09
ORD IDord-4fa3682e809143808febe4020a6f42f7
Source noteuspto-grants-2002_09