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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529540Generated: October 30, 2026

Hydrochloric Acid → (4S,7S,10aS)-4-Amino-7-(methoxymethyl)hexahydro-2H-pyrido[2,1-b][1,3]thiazepin-5(7H)-one hydrochloride

https://huagongshe.com/reaction/529540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-butyl (4S,7S,10aS)-7-(methoxymethyl)-5-oxooctahydro-2H-pyrido[2,1-b][1,3]thiazepin-4-ylcarbamateHCID 86706224—
Product(4S,7S,10aS)-4-Amino-7-(methoxymethyl)hexahydro-2H-pyrido[2,1-b][1,3]thiazepin-5(7H)-one hydrochlorideHCID 6829274193%

Reaction Steps

A solution of HCl (4.0 N in dioxane, 1 mL) was added to a reaction flask containing tert-butyl (4S,7S,10aS)-7-(methoxymethyl)-5-oxooctahydro-2H-pyrido[2,1-b][1,3]thiazepin-4-ylcarbamate (83 mg, 0.24 mmol). The reaction mixture was then stirred at rt overnight. The reaction mixture was concentrated. Ether was added to the residue. A white solid formed. The mixture was stirred for 5 min and then filtered. The solid was dried under vacuum to give (4S,7S,10aS)-4-Amino-7-(methoxymethyl)hexahydro-2H-pyrido[2,1-b][1,3]thiazepin-5(7H)-one hydrochloride (63 mg, 0.22 mmol, 93% yield) as a white solid. Anal. Calcd. for C11H20N2O2S m/z 244.4. found: 245.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346852B2
Source datasetuspto-grants-2016_05
ORD IDord-b56a3aa2acf74799ab0a3264d4856b2f
Source noteuspto-grants-2016_05