Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719919Generated: October 30, 2026

Sodium methanethiolate → (5-Methylsulfanylmethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/719919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactanttert-Butyl (5-(bromomethyl)pyrazin-2-yl)carbamateHCID 45073740—
SolventAcetoneHCID 180—
Product(5-Methylsulfanylmethyl-pyrazin-2-yl)-carbamic acid tert-butyl esterHCID 67482522—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (5-bromomethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester (prepared according to WO 02/070494, 1.03 g, 3.575 mmol) in acetone (11.6 mL) was treated with sodium thiomethoxide (0.33 g, 4.473 mmol). The reaction mixture was stirred at 25° C. for 5 h 15 min. The reaction was then concentrated in vacuo, and the residue was partitioned between ethyl acetate (200 mL) and water (200 mL). The aqueous layer was back-extracted with ethyl acetate (100 mL). The combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40L, Silica, 5% ethyl acetate/methylene chloride) afforded (5-methylsulfanylmethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester as a crude white solid (0.45 g, 49%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132425B2
Source datasetuspto-grants-2006_11
ORD IDord-88bd57ef58ec4f9ba95c336acb1792e7
Source noteuspto-grants-2006_11