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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424393Generated: November 3, 2026

Diisopropylethylamine → (4-fluorophenyl)(4-(5-methyl-1H-pyrazol-3-ylamino)quinazolin-2-yl)methanone

https://huagongshe.com/reaction/1424393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
Reactant(4-Chloroquinazolin-2-yl)(4-fluorophenyl)methanoneHCID 86649048—
SolventDimethylformamideHCID 6228—
Product(4-fluorophenyl)(4-(5-methyl-1H-pyrazol-3-ylamino)quinazolin-2-yl)methanoneHCID 4689224329%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of (4-chloroquinazolin-2-yl)(4-fluorophenyl)methanone (84 mg, 0.30 mmol) in DMF (3 mL) were added DIEA (0.103 mL, 0.6 mmol) and 5-methyl-1H-pyrazol-3-amine (88 mg, 0.9 mmol at rt. The reaction mixture was heated at 40° C. overnight. The reaction was quenched by adding water and the yellow precipitate was collected by filtration and washed with water. The crude product was purified by silica gel chromatography eluting with DCM/MeOH to give (4-fluorophenyl)(4-(5-methyl-1H-pyrazol-3-ylamino)quinazolin-2-yl)methanone (30 mg, 29%). 1H NMR (300 MHz, DMSO-d6) δ 2.19 (s, 3H), 6.54 (s, 1H), 7.40 (m, 2H), 7.68 (t, 1H), 7.9-7.7 (m, 2H), 8.08 (m, 2H), 8.74 (d, 1H), 10.66 (s, 1H), 12.20 (s, 1H); LC-MS (ESI) m/z 348 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927711B2
Source datasetuspto-grants-2015_01
ORD IDord-e474666f5ab44c5f98edc630548a6ae2
Source noteuspto-grants-2015_01