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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441544Generated: November 1, 2026

Hydrochloric Acid → HCID 59164422, compound

https://huagongshe.com/reaction/1441544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantMethanesulfonohydrazideHCID 269268—
ReactantHCID 67390427HCID 67390427—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59164422HCID 5916442279%

Reaction Steps

A solution of 2-methyl-5-propionyl-4-trifluoromethyl-benzoic acid methyl ester (180 mg, 0.65 mmol) in THF (2.6 mL) was treated with (CCl3O)2CO (65.3 mg, 0.22 mmol) at r.t. under argon. The mixture was stirred for 15 min and Et3N (91 μL, 0.65 mmol) was added. The suspension was stirred for another 3 h and CH3SO2NHNH2 (73.5 mg, 0.65 mmol) was added. After 20 h, an aqueous solution of sodium hydroxide (1N, 0.87 mL) was added and the yellow suspension was stirred for 4 h at r.t. The pH of the mixture was then adjusted to 4-5 with an aqueous solution of hydrochloric acid (1N), and it was then diluted with EtOAc. The layers were separated and the organic phase was washed once with water, once with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was recrystallized in DCM to give N-(2,4-dioxo-6-propionyl-7-trifluoromethyl-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide (195 mg, 0.51 mmol, 79%) as a white solid, m.p. 234-236° C., ESI-MS: m/z 380 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655666B2
Source datasetuspto-grants-2010_02
ORD IDord-5fc11eab7a5e4de485c954bfc5853c5e
Source noteuspto-grants-2010_02