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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040849Generated: October 30, 2026

1-Ethyl-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-one → 2H-1-Benzazepin-2-one, 8-amino-1-ethyl-1,3,4,5-tetrahydro-

https://huagongshe.com/reaction/1040849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-oneHCID 9834583—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2H-1-Benzazepin-2-one, 8-amino-1-ethyl-1,3,4,5-tetrahydro-HCID 9899166101%

Reaction Steps

To a solution of 1-ethyl-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-one (920 mg, 3.9 mmol, WO2002100327A2) in EtOH (13 mL) was sequentially added 10% Pd/C (155 mg) and hyrdrazine-monohydrate (3 mL). The solution was warmed to reflux for 2.5 h, cooled, filtered through celite, and repeatedly evaporated from toluene to remove residual hydrazine to afford 8-amino-1-ethyl-1,3,4,5-tetrahydro-benzo[b]azepin-2-one (805 mg, 100%) that had the following properties: LC/MS (ESI+): 205 (M+H); 1H-NMR (CDCl3, 400 MHz): δ 6.97 (d, J=7.8, 1H), 6.55 (s, 1H), 6.52 (d, J=7.8, 1H), 3.95 (br s, 2H), 3.67 (br s, 2H), 2.60 (br s, 2H), 2.29 (m, 2H), 2.11 (m, 2H), 1.15 (t, J=6.2, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-dc7ec6fb35ea4878b08e190d58d83555
Source noteuspto-grants-2013_10