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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764855Generated: November 2, 2026

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

https://huagongshe.com/reaction/1764855

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 numberUSRE039679E1
Source datasetuspto-grants-2007_06
ORD IDord-a6b59260816c4fd4a55f0f2266cdfe04
Source noteuspto-grants-2007_06