Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719920Generated: October 30, 2026

Trifluoroacetic acid → 5-Methylsulfanylmethyl-pyrazin-2-ylamine

https://huagongshe.com/reaction/719920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(5-Methylsulfanylmethyl-pyrazin-2-yl)-carbamic acid tert-butyl esterHCID 67482522—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 149230.1%
Product5-Methylsulfanylmethyl-pyrazin-2-ylamineHCID 21897339201.9%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (5-methylsulfanylmethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester (0.45 g, 1.762 mmol) in methylene chloride (18 mL) was treated with trifluoroacetic acid (1.4 mL, 18.172 mmol) and then was stirred at 25° C. for 2 h 15 min. The reaction solution was then treated with a second aliquot of trifluoroacetic acid (0.7 mL, 9.086 mmol) and was stirred at 25° C. for 5 h. At this time, the reaction mixture was concentrated in vacuo. Biotage chromatography (FLASH 40S, Silica, 1/9 methanol/methylene chloride with 0.1% ammonium hydroxide) afforded 5-methylsulfanylmethyl-pyrazin-2-ylamine (276.1 mg, quant.) as a white solid: mp 102.0–102.7° C.; EI-HRMS m/e calcd for C6H9N3S (M+) 155.0517, found 155.0516.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132425B2
Source datasetuspto-grants-2006_11
ORD IDord-4e9e437dc3bf4b389f8d3d4843900b0f
Source noteuspto-grants-2006_11