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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108110Generated: November 2, 2026

HCID 10414055, compound → HCID 23045029, compound

https://huagongshe.com/reaction/2108110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10414055HCID 10414055—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 23045029HCID 23045029—

Reaction Steps

A mixture of 1-(7,8-dimethoxy-2,3-dihydro-1-benzoxepin4-ylcarbonyl)-4-(3,4,5-trimethoxybenzoyl)piperazine obtained in Working Example 26 (0.5 g) and methanol (20 ml) is stirred under a hydrogen stream in the presence of 10% palladium-carbon (0.3 g) under atmospheric pressure at room temperature for 10 hours. After filtration of the catalyst, the filtrate is concentrated under reduced pressure. The residue is dissolved in ethyl acetate. The resulting solution is washed with water, dried and concentrated in vacuo. The residue is tritutated with ethyl ether and the resulting powder is filtered off to give 1-(7,8-dimethoxy2,3,4,5-tetrahydro-1-benzoxepin-4-ylcarbonyl)-4-(3,4,5-trimethoxybenzoyl)piperazine as a colorless powder (0.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04937246
Source datasetuspto-grants-1990_06
ORD IDord-13c9d9012dfb49f98f3e4bf11c9aec6a
Source noteuspto-grants-1990_06