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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421215Generated: November 3, 2026

HCID 70296521, compound → HCID 54028746, compound

https://huagongshe.com/reaction/1421215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70296521HCID 70296521—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 54028746HCID 54028746142.8%

Reaction Steps

1.2 g (3.56,mmoles) of 1-(4-aminostyryl)-4-methyl-7,8-dimethoxy-3,4-dihydro-5H-2,3-benzodiazepine prepared according to Example 33 is suspended in 6 ml of acetic anhydride. The suspension is stirred for 1 hour at room temperature. In the meantime the starting compound gets dissolved, the end-product begins to separate and the reaction mixture gets thick. The separated product is filtered off, washed three times with 15 ml each of diethyl ether and dried at a temperature between 80° C. and 100° C. Thus 1.07 g (71.3%) of the desired compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06075018
Source datasetuspto-grants-2000_06
ORD IDord-f4174ff51da241c1813447c69df03813
Source noteuspto-grants-2000_06