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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424436Generated: November 1, 2026

Diisopropylethylamine → HCID 66613954, compound

https://huagongshe.com/reaction/1424436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
ReactantHCID 86649058HCID 86649058—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66613954HCID 6661395483%

Reaction Conditions

Temperature40 °C

Reaction Steps

To (7-(benzyloxy)-4-chloroquinazolin-2-yl)(4-fluorophenyl)methanone (380 mg, 0.97 mmol) in DMF (10 mL) at rt were added DIEA (500 uL, 2.90 mmol), 5-methyl-1H-pyrazol-3-amine (280 mg, 2.90 mmol), and KI (161 mg, 0.97 mmol). After stirring at 40° C. for 18 h, the solution was cooled and diluted with water. After standing at 0° C. for 1 h, the precipitate was collected by filtration and dried under reduced pressure to afford (7-(benzyloxy)-4-(5-methyl-1H-pyrazol-3-ylamino)quinazolin-2-yl)(4-fluorophenyl)methanone as a yellow solid (365 mg, 83%) 1H NMR (300 MHz, DMSO-d6) δ ppm 2.18 (s, 3H) 5.30 (s, 2H) 6.48 (s, 1H) 7.33-7.44 (m, 8H) 7.50-7.52 (m, 2H) 8.07 (m, 2H) 8.65 (m, 1H) 10.53 (s, 1H) 12.18 (s, 1H). LC-MS (ESI) m/z 454 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927711B2
Source datasetuspto-grants-2015_01
ORD IDord-f2d45a210b634eca9886faee16795dcf
Source noteuspto-grants-2015_01