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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911406Generated: October 30, 2026

Water → HCID 57656171, compound

https://huagongshe.com/reaction/911406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57655927HCID 57655927—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 57656171HCID 5765617158.6%

Reaction Steps

Dissolve 3-(t-butoxycarbonyl)-7-chloro-6-(thiazol-5-ylmethyleneamino)-2,3,4,5-tetrahydro-1H-benzo[d]azepine (228 mg, 0.58 mmol) in methanol (10 mL), add sodium borohydride (263 mg, 7 mmol) and reflux for 28 h. Cool to ambient temperature, dilute with EtOAc and add slowly water. Separate the organic layer, extract the aqueous layer three times with EtOAc. Combine the organic extracts, dry over Na2SO4, filter and concentrate in vacuo. Purify by chromatography on silica gel eluting with EtOAc/hexane (1:3) to give the desired intermediate as a colorless oil (134 mg, 58%). MS (ES+) m/z: 394 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-49eeeeb939aa4710af11a23cb0732d7f
Source noteuspto-grants-2011_09