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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529557Generated: October 30, 2026

Trifluoroacetic acid → (4S,7R,10aS)-4-amino-7-ethylhexahydro-2H-pyrido[2,1-b][1,3]thiazepin-5(7H)-one trifluoroacetate

https://huagongshe.com/reaction/529557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl (4S,7R,10aS)-7-ethyl-5-oxooctahydro-2H-pyrido[2,1-b][1,3]thiazepin-4-ylcarbamateHCID 86706235—
SolventDichloromethaneHCID 6344—
Product(4S,7R,10aS)-4-amino-7-ethylhexahydro-2H-pyrido[2,1-b][1,3]thiazepin-5(7H)-one trifluoroacetateHCID 86706236100%

Reaction Steps

To a solution of tert-butyl (4S,7R,10aS)-7-ethyl-5-oxooctahydro-2H-pyrido[2,1-b][1,3]thiazepin-4-ylcarbamate (52 mg, 0.16 mmol) in DCM (1 mL) was added TFA (1.0 mL, 13 mmol). The reaction mixture was stirred at rt for 1 hr. The reaction mixture was concentrated and dried under high vacuum to afford (4S,7R,10aS)-4-amino-7-ethylhexahydro-2H-pyrido[2,1-b][1,3]thiazepin-5(7H)-one trifluoroacetate (54 mg, 0.16 mmol, 100% yield) as an oil. Anal. Calcd. for C11H20N2OS m/z 228.3. found: 229.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346852B2
Source datasetuspto-grants-2016_05
ORD IDord-3b1c492c4e3348f6ba886c67b1ca8c3e
Source noteuspto-grants-2016_05