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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649847Generated: November 1, 2026

Methyl Isocyanate → 2-(3-Methylureido)-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole

https://huagongshe.com/reaction/1649847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazoleHCID 19854937—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Methylureido)-4-[4-(diphenylmethoxy)piperidinomethyl]thiazoleHCID 14500901—

Reaction Steps

To a stirred solution of 2-amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole (1.0 g) in dry tetrahydrofuran (10 ml) was added dropwise methyl isocyanate (0.34 ml) at ambient temperature. After the addition had been completed, the reaction mixture was stirred for 3 hours. 1N Sodium hydroxide solution (3 ml) was added thereto and stirring was continued for 30 minutes. The reaction mixture was concentrated under reduced pressure and the residue was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After removal of solvent, the residue was subjected to column chromatography on silica gel and eluted with a mixture of chloroform and methanol (20:1 V/V). The fractions containing the object compound were combined and concentrated under reduced pressure. The residue was triturated with 70% ethanol to give white powder. Recrystallization from 70% ethanol gave 2-(3-methylureido)-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921887
Source datasetuspto-grants-1990_05
ORD IDord-a68b5fc93212480e9732c0ce195339f9
Source noteuspto-grants-1990_05