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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359645Generated: October 28, 2026

Methyl iodide → Ethyl 2-[(tert-butoxycarbonyl)(methyl)amino]-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1359645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-((tert-butoxy(hydroxy)methylidene)amino)-1,3-thiazole-5-carboxylateHCID 7213140—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-[(tert-butoxycarbonyl)(methyl)amino]-1,3-thiazole-5-carboxylateHCID 2235081545%

Reaction Steps

A flask is charged with a suspension of sodium hydride (60% in mineral oil) (0.109 g, 2.72 mmol) in THF (5 mL). The ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylate (0.735 g, 2.70 mmol) is added, followed by iodomethane (175 μL, 2.70 mmol) and the resulting suspension is heated to reflux for 3 hours, then cooled to room temperature. Water is added, followed by 1.0 N NaOH. The basic phase is extracted with 3 portions of EtOAc. The combined organic phases are washed with brine, dried over Na2SO4, filtered, and concentrated to give a clear oil purified with flash chromatography. Yield 45%. HRMS (FAB) calculated for C12H18N2O4S+H 287.1065, found 287.1068.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599916B2
Source datasetuspto-grants-2003_07
ORD IDord-df0149df9a754687b6dbd6361dabb8cb
Source noteuspto-grants-2003_07