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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251413Generated: October 29, 2026

Acetyl chloride → HCID 24957540, compound

https://huagongshe.com/reaction/251413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant4-{4-Chloro-6-[4-(methylsulfonyl)phenyl]-2-(trifluoromethyl)pyrimidin-5-yl}benzenesulfonamideHCID 86613620—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 24957540HCID 24957540—

Reaction Conditions

Temperature30 °C

Reaction Steps

A solution of 4-{4-chloro-6-[4-(methylsulfonyl)phenyl]-2-(trifluoromethyl)pyrimidin-5-yl}benzenesulfonamide (0.5 g, 1.01 mmol, prepared according to the procedure described in PCT/IB03/02879), DMAP (0.01 g) and acetyl chloride (0.5 g, 6.36 mmol) were stirred at 30° C. TLC confirmed the completion of the reaction after 4 hours of stirring under the same conditions. Subsequently the resulting mass was poured onto the ice, and the procedure described for example 14 was followed to afford the title compound (0.252 g, 46.41%, purity by HPLC 98.82%); m.p.: 230-235° C. 1H-NMR (DMSO-d6) δ: 1.87 (s, 3H), 3.17 (s, 3H), 7.51-7.53 (m, 2H), 7.66-7.67 (m, 2H), 7.8-7.82 (d, 2H), 7.9 (s, 1H), 7.99 (s, 1H), 12.14 (s, 1H, D2O exchangeable). IR (KBr) cm−1: 3150, 1720, and 1525. MS m/z: 533.7(M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863446B2
Source datasetuspto-grants-2011_01
ORD IDord-b2555760740143a1b7628b2399a64324
Source noteuspto-grants-2011_01