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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520440Generated: October 25, 2026

Pyridine-3-sulfonyl chloride hydrochloride → N-(3-methyl-4-oxo-2-phenyl-3,4-dihydroquinazolin-8-yl)pyridine-3-sulfonamide

https://huagongshe.com/reaction/520440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
Reactant8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-oneHCID 58552822—
SolventPyridineHCID 1049—
ProductN-(3-methyl-4-oxo-2-phenyl-3,4-dihydroquinazolin-8-yl)pyridine-3-sulfonamideHCID 6799319462.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

Pyridine-3-sulfonyl chloride hydrochloride 7 (280 mg, 1.3 mmol) was added to a solution of 8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-one 5 (100 mg, 0.313 mmol) in pyridine (5 mL). The reaction mixture was heated at 80° C. for 12 h. The pyridine was removed in vacuo. The residue was taken up in CH2Cl2, washed with sat. aq NaHCO3, dried (MgSO4) and concentrated. The crude residue was purified by MPLC eluting with CH2Cl2/MeOH (0-10%) followed by recrystallization from CH3CN to give Compound 361 (77 mg, 53% yield). MS (ESI) calcd for C21H15F3N4O3S: 460.08. found: 461 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326986B2
Source datasetuspto-grants-2016_05
ORD IDord-4b14d276c9464054b64576a01ecda094
Source noteuspto-grants-2016_05