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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354031Generated: October 30, 2026

Ethyl isothiocyanate → Methyl 5-(ethylamino)-2-(methylthio)-4-thiazolecarboxylate

https://huagongshe.com/reaction/354031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isothiocyanateHCID 10966—
ReactantN-[Bis(methylthio)methylene]glycine methyl esterHCID 5007923—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-(ethylamino)-2-(methylthio)-4-thiazolecarboxylateHCID 22280379—

Reaction Steps

A solution of N-[Bis(methylthio)methylene]glycine methyl ester (1 mmole) in anhydrous THF (2 mL) was added to a solution of t-BuOK (1.4 mmole) in anhydrous THF (10 mL) at −78° C. and the mixture was stirred for 30 min. Then a solution of ethyl isothiocyanate (1 mmole) in anhydrous THF (2 mL) was added and the reaction was stirred at −78° C. for 30 min and at room temperature for 2 h. The reaction was quenched with water. Extraction and chromatography gave 2-methylthio-5-(N-ethylamino)-4-methoxycarbonylthiazole as a yellow solid, which was subjected to Step B and C of Example 18 followed by Step C of Example 3 to give 2-methylthio-5-(N-ethylamino)-4-phosphonomethoxycarbonylthiazole (18.4) as a solid. Mp>200° C. (decomp). Anal. Calcd. for C8H13N2O5PS2+0.1 HBr: C: 29.99; H: 4.12; N: 8.74. Found: C: 29.71; H: 4.10; N: 8.60.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756360B1
Source datasetuspto-grants-2004_06
ORD IDord-bb353c4d4ccf495987f63bd4e593a500
Source noteuspto-grants-2004_06