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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981889Generated: November 1, 2026

Sodium hydride → 6-t-Butoxycarbonylamino-4-N-(carbomethoxymethyl)-perhydro-1,4-thiazepin-5-one

https://huagongshe.com/reaction/1981889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl IodoacetateHCID 6429536—
Reactant(Hexahydro-5-oxo-1,4-thiazepin-6-yl)carbamic acid, (1,1-dimethylethyl) esterHCID 15591256—
SolventTetrahydrofuranHCID 8028—
Product6-t-Butoxycarbonylamino-4-N-(carbomethoxymethyl)-perhydro-1,4-thiazepin-5-oneHCID 1363373269.6%

Reaction Steps

6-t-Butoxycarbonylamino-perhydro-1,4-thiazepin-5-one (0.1 g) and methyl iodoacetate (0.1 g) are dissolved in 1 ml of THF. Sodium hydride (50% suspension in oil) is added in batches. After one hour at room temperature, the reaction is quenched with 2 ml of 10% ammonium chloride solution. The crude product is extracted into methylene chloride, and subsequently chromatographed on silica gel (40:1 chloroform-methanol) to yield the pure product (0.09 g). The NMR spectrum is consistent with the assigned structure. A sample is obtained by recrystallization from ether-methanol and analyzes for C13H22N2O5S.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04594341
Source datasetuspto-grants-1986_06
ORD IDord-636097863177492da31dfa4e441736f9
Source noteuspto-grants-1986_06