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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356373Generated: November 3, 2026

Sodium cyanoborohydride → HCID 69896056, compound

https://huagongshe.com/reaction/1356373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22396798HCID 22396798—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 69896056HCID 69896056—

Reaction Conditions

Temperature0 °C

Reaction Steps

10-(4-Chlorophenyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole hydrochloride (140 mg) was dissolved in TFA (3 ml), cool to 0° C. and sodium cyanoborohydride was added portionwise (150 mg). The reaction mixture stirred two hours, was quenched with 2N NaOH, extracted with EtOAc, dried over MgSO4, filtered and concentrated. The product was dissolved in EtOAc and 1N HCl in Et2O was added. The solvent was evaporated and solid recrystallized from EtOAc/MeOH to provide the title compound: 1H NMR (DMSO-d6) δ 1.31, 1.66, 2.21, 2.7, 2.91, 3.03, 3.27, 4.1-4.4, 6.88, 7.25, 7.52. HRMS (FAB) calcd for C18H21ClN12 (MH+) 299.1315, found 299.1321.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586421B2
Source datasetuspto-grants-2003_07
ORD IDord-a3d26c8da2bc4bd990bcb7cb999b4d43
Source noteuspto-grants-2003_07