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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50979Generated: October 29, 2026

Water → 3,4-Dihydro-1,5-benzothiazepin-5(2h)-amine

https://huagongshe.com/reaction/50979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12233800HCID 12233800—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product3,4-Dihydro-1,5-benzothiazepin-5(2h)-amineHCID 1223380259.1%

Reaction Steps

A solution of 5-nitroso-2,3,4,5-tetrahydro-1,5-benzothiazepine (32.21 g, 0.166 mol) in THF (650 mL) was added dropwise to LAH (1.0M in THF, 166 mL) under N2 such that the temperature did not rise above 27-29° C. Once the addition was complete, the mixture was stirred at room temperature for 1 hr. It was cooled in an ice bath and treated with H2O (7.3 mL) added dropwise, followed by 1N NaOH (32.4 mL). Once at room temperature, the mixture was filtered and the filtrate was evaporated under reduced pressure. The residue was taken up in CH2Cl2 (200 mL) washed with H2O, and dried over MgSO4, and stripped of solvent under reduced pressure to yield 29.42 g (98%) of the crude product. Purification by column chromatography (EtOAc) afforded 17.69 g (59% yield) of 3,4-dihydro-1,5-benzothiazepin-5(2H)-amine as a liquid which was converted to the HCl salt, m.p. 202° C. (decomposition). (M+H)+ 180.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713471B1
Source datasetuspto-grants-2004_03
ORD IDord-c28e810b48384baba252a0909a1fc62c
Source noteuspto-grants-2004_03