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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12233800 | HCID 12233800 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Dihydro-1,5-benzothiazepin-5(2h)-amine | HCID 12233802 | 59.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713471B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-c28e810b48384baba252a0909a1fc62c |
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| Source note | uspto-grants-2004_03 |
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