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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307047Generated: November 1, 2026

8,9-Dichloro-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole → HCID 59075499, compound

https://huagongshe.com/reaction/2307047

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8,9-Dichloro-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoleHCID 22609204—
SolventMethanolHCID 887—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 59075499HCID 5907549936%

Reaction Steps

A solution of 8,9-dichloro-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (0.40 g, 1.6 mmol) in TFA (4.0 mL) was cooled to 0° C., then a freshly prepared solution of Na(CN)BH3 (0.49 g, 7.8 mmol) in MeOH (.1.5 mL) was added dropwise. The ice bath was removed after the addition was complete. After 2.5 h, the reaction was diluted with H2O, made basic with 50% aqueous NaOH, and extracted with EtOAc. The combined organic extracts were washed with brine, dried over Na2SO4, decanted, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography and prep HPLC to give 0.14 g (36%) of the title compound as pale orange solid. 1H NMR (d-CHCl3) δ 7.00, 6.58, 4.22, 3.81, 3.58, 3.14-2.98, 2.79, 2.07-1.87: IR (drift) 3201, 3170, 3149, 3031, 2927, 2852, 2838, 2750, 1608, 1483, 1450, 1365, 1273, 832, 660 cm−1; HRMS (FAB) calcd for C12H14Cl2N2+H 257.0612, found 257.0614.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828314B2
Source datasetuspto-grants-2004_12
ORD IDord-d96d008378ad4fc59fbfa4bb328378ff
Source noteuspto-grants-2004_12