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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307056Generated: November 3, 2026

Sodium cyanoborohydride → HCID 69896056, compound

https://huagongshe.com/reaction/2307056

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 (140mg) 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 C18H21ClN2 (MH+) 299.1315, found 299.1321.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828314B2
Source datasetuspto-grants-2004_12
ORD IDord-faa9d1b496e64337aed4983505ffe831
Source noteuspto-grants-2004_12