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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187559Generated: October 31, 2026

7-nitro-3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-1,5-methano-3-benzazepine → 3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-1,5-methano3-benzazepin-7-amine

https://huagongshe.com/reaction/2187559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-nitro-3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-1,5-methano-3-benzazepineHCID 21864705—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-1,5-methano3-benzazepin-7-amineHCID 2186471694.5%

Reaction Steps

Hydrogenation of 1-(4-nitro-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)2.2.2-trifluoro-ethanone (2.0 g, 6.66 mmol) under a H2 atmosphere (40 psi) and 10% Pd/C (200 mg) in MeOH over 1.5 hours, filtration through Celite and concentration affords a yellow oil (1.7 g). (TLC 50% EtOAc/hexanes Rf0.27). 1H NMR (400 MHz, CDCl3) δ6.99 (m, 1H), 6.64 (br s, 1H), 6.57 (m, 1H), 4.25 (m, 1H), 3.82 (m, 1H), 3.50 (m, 1H), 3.17-3.07 (m, 3H), 2.35 (m, 1H), 1.90 (d, J=10.8 Hz, 1H). GCMS m/e 270 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410550B1
Source datasetuspto-grants-2002_06
ORD IDord-d0a708b849ec4d2cb50123b9ff716a73
Source noteuspto-grants-2002_06