Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657005Generated: October 29, 2026

Methanesulfonyl chloride → HCID 15729206, compound

https://huagongshe.com/reaction/1657005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15729159HCID 15729159—
SolventPyridineHCID 1049—
ProductHCID 15729206HCID 1572920643.8%

Reaction Steps

To a solution of 2-amino-5-(2-pyrimidinylthio)thiazole (1.0 g) in a pyridine (20 ml) was dropwise added methanesulfonyl chloride (0.8 ml) at 5° C. with stirring. The mixture was stirred at room temperature for 24 hours. The reaction mixture was concentrated under reduced pressure and water was added to this residue. The mixture was extracted with a mixture of tetrahydrofuran and ethyl acetate (1:1), washed with aqueous saturated sodium chloride and dried over magnesium sulfate. The solution was concentrated under reduced pressure to give solid. The solid was recrystallized from 50% ethanol to give 2-methanesulfonylamino-5-(2-pyrimidinylthio)thiazole (0.60 g, yield: 43.8%). mp: 200° C. (dec.) IR (Nujol): 3120, 1585, 1545, 1440, 1305, 1140 cm-1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-ca661e29d0ad46669c4d9db30f576201
Source noteuspto-grants-1993_10