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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037685Generated: October 31, 2026

Thionyl Chloride → 2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzenesulfonyl chloride

https://huagongshe.com/reaction/1037685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzenesulfonic acidHCID 58457204—
CatalystDimethylformamideHCID 6228—
Product2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzenesulfonyl chlorideHCID 58457194—

Reaction Conditions

Temperature22 °C

Reaction Steps

40 ml of thionyl chloride together with one drop of DMF are added to a solution of 5 g of 2-[2-amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzenesulfonic acid. The mixture is stirred at 22° C. for 16 h, evaporated in vacuo, taken up in 500 ml of DCM and extracted twice with 300 ml of water each time. The organic phase is dried over magnesium sulfate, filtered off and evaporated to dryness in vacuo. The residue is employed in the following steps without further purification. Yield: 6.9 g (98%) of 2-[2-amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzenesulfonyl chloride;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546565B2
Source datasetuspto-grants-2013_10
ORD IDord-c24e899b52594806b5760e2434585fc2
Source noteuspto-grants-2013_10