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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370362Generated: October 31, 2026

3-Benzyl-10-phenyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole → 10-Phenyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole

https://huagongshe.com/reaction/1370362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyl-10-phenyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoleHCID 22396727—
CatalystAcetic AcidHCID 176—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product10-Phenyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoleHCID 22396807121.7%

Reaction Steps

A mixture of 3-benzyl-10-phenyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (0.22 g, 0.62 mmol), glacial acetic acid (2 drops) and Pd/C (10%, 0.11 g) in ethanol (50.0 mL) was reacted in a manner similar to Example 8 to give 0.198 g (90%) of a brown foam. Crystallization from ethyl acetate gave 0.030 g of the title compound as a beige solid: mp>250° C.; 1H NMR (300 MHz, CDCl3) δ 7.97, 7.48-7.36, 7.16, 6.94, 3.12-3.08, 3.02-2.98, 2.87-2.83, 2.47-2.43; IR (drift) 3053, 3025, 2927, 2895, 2833, 1458, 1428, 1415, 1335, 1292, 1262, 790, 760, 751, 703 cm−1; MS (EI) m/z 262 (M+); HRMS (FAB) calcd for C18H18N2+H: 263.1548, found 263.1550.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583135B2
Source datasetuspto-grants-2003_06
ORD IDord-7f567dbbd4d140ce89470d82ced63cb8
Source noteuspto-grants-2003_06