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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258669Generated: November 1, 2026

Chlorosulfonic acid → 3-Amino-8-bromo-5,6-dihydrobenzo[f]quinazolin-1(2h)-one-9-sulfonylchloride

https://huagongshe.com/reaction/2258669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant3-amino-8-bromo-5,6-dihydrobenzo[f]quinazolin-1(2H)-oneHCID 135838183—
Product3-Amino-8-bromo-5,6-dihydrobenzo[f]quinazolin-1(2h)-one-9-sulfonylchlorideHCID 136120935104.3%

Reaction Steps

Chlorosulfonic acid(100 g) was added to 3-amino-8-bromo-5,6-dihydrobenzo[f]quinazoline-1(2H)-one (5.20 g,17.8 mmole) and the solution stirred overnight at room temperature. The reaction mixture was poured over ice, the collected solid washed with water, and dried under high vacuum to give 3-amino-8-bromo-5,6-dihydrobenzo[f]quinazolin-1(2H)-one-9-sulfonyl chloride(7.25 g,90%). 1H NMR (DMSO-d6, 200 MHz) δ: 2.67-2.75 (m, 2H, Ar CH2), 2.81-2.88 (m, 2H, Ar CH2), 7.43 (s, 1H, Ar), 8.23 (br s, 2H, NH2), 8.91(s, 1H, Ar), 99.0-10.50 (v br s, 1H, NH). Anal Calculated for C12H9BrClN3O3S 1/2 H2O.9/20 H2SO4 : C,32.48; H,2.48; N,9.47; S,10.46. Found: C,32.68; H,2.37; N,9.20; S,10.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661155
Source datasetuspto-grants-1997_08
ORD IDord-98aca83359804a8fbb48eb6c7a51f95a
Source noteuspto-grants-1997_08