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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271070Generated: November 2, 2026

Acetic Anhydride → HCID 11375081, compound

https://huagongshe.com/reaction/1271070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantEntasobulinHCID 10203597—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 11375081HCID 11375081—

Reaction Steps

0.833 g (6.82 mMol) of DMAP, 1.38 g (13.6 mMol) of triethylamine and 13.9 g (136 mMol) of acetic anhydride are added, under nitrogen, to a stirred solution of 6.0 g (13.6 mMol) of 2-[1-(4-chlorobenzyl)-1H-indol-3-yl]-2-oxo-N-quinolin-6-ylacetamide in 60 ml of DMF. The reaction mixture is stirred at room temperature for 10 minutes and, after that, poured into 200 ml of ethyl acetate. After 300 ml of water have been added, the mixture is shaken in a separating funnel after which the two phase separate. Precipitation begins after 20 minutes. The pale yellow crystals are filtered off and dried in vacuo at 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205299B2
Source datasetuspto-grants-2007_04
ORD IDord-cd002fb98cc54947b11cb988e0813ee5
Source noteuspto-grants-2007_04