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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155944Generated: October 31, 2026

Hydrochloric Acid → 2-Acetyl-N-[(4-methylquinazolin-2-yl)aminocarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/1155944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantN-[(4-Methylquinazolin-2-yl)aminocarbonyl]-2-carboxybenzenesulfonamideHCID 20536263—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-Acetyl-N-[(4-methylquinazolin-2-yl)aminocarbonyl]benzenesulfonamideHCID 20536259—

Reaction Steps

A mixture containing 0.86 g of N-[(4-methylquinazolin-2-yl)aminocarbonyl]-2-carboxybenzenesulfonamide in 50 ml of anhydrous tetrahydrofuran is treated with 40 ml of a 1.4 M solution of methyllithium in ether at 25° under a nitrogen atmosphere. The mixture is stirred for 4 hours at ambient temperature and then poured into 500 ml of water containing 10 ml of concentrated hydrochloric acid. The product can be isolated by extraction into methylene chloride followed by evaporation and if necessary, can be purified by preparative thin layer chromatography and/or recrystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04333760
Source datasetuspto-grants-1982_06
ORD IDord-6e969edd3f8444ca9ced5c613cc35a6d
Source noteuspto-grants-1982_06