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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603132Generated: November 2, 2026

HCID 19608103, compound → HCID 19607940, compound

https://huagongshe.com/reaction/1603132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19608103HCID 19608103—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 19607940HCID 1960794047.2%

Reaction Steps

5-Azidomethyl-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.27 g) is suspended in ethanol (50 ml) and the mixture is subjected to catalytic hydrogenation at room temperature under 3 kg/cm2 for 6 hours by using 10% Pd-C (27 mg). The catalyst is removed by filtration with celite and the filtrate is distilled off and the resulting residue is recrystallized from ethanol to give 5-aminomethyl-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.12 g) as colorless needles, m.p. 233-235° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05985869
Source datasetuspto-grants-1999_11
ORD IDord-7e17cb8c1e3448aa8a2b5e79d3fb8e89
Source noteuspto-grants-1999_11