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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654362Generated: October 25, 2026

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

https://huagongshe.com/reaction/1654362

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] quinazolin-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), 9.90-10.50 (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 numberUS05405851
Source datasetuspto-grants-1995_04
ORD IDord-5624e31c3a734c119a083a3d22407b6e
Source noteuspto-grants-1995_04