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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381997Generated: October 28, 2026

Acetic Anhydride → HCID 21934354, compound

https://huagongshe.com/reaction/381997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 10297455HCID 10297455—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 21934354HCID 21934354—

Reaction Steps

A mixture of 2-(4-fluorophenyl)-4-(3-hydroxy-3-methyl-1-butoxy)-5-[4-(aminosulfonyl)phenyl]-3(2H)-pyridazinone (Example 470, 1 equivalent), acetic anhydride (3 equivalents), 4-(dimethylamino)pyridine (0.3 equivalents), and triethylamine (1.2 equivalents) is stirred at room temperature for 16 hours. The reaction mixture is partitioned between ethyl acetate and water. The organic layer is washed with brine then dried over MgSO4 and filtered. The filtrate is concentrated in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307047B1
Source datasetuspto-grants-2001_10
ORD IDord-6608009422154fb1ba8ab20854a9ba12
Source noteuspto-grants-2001_10