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HRID 625743作成日:2026年10月26日

Methanol → 3-(2-(4-fluorobenzoyl)quinazolin-4-ylamino)-1H-pyrazole-5-carbonitrile

https://huagongshe.com/reaction/625743

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物5-Amino-1H-pyrazole-3-carbonitrileHCID 21180574—
反応物(4-Chloroquinazolin-2-yl)(4-fluorophenyl)methanoneHCID 86649048—
溶媒DimethylformamideHCID 6228—
生成物3-(2-(4-fluorobenzoyl)quinazolin-4-ylamino)-1H-pyrazole-5-carbonitrileHCID 5684854623.5%

反応手順

A mixture of (4-chloroquinazoline-2-yl)(4-fluorophenyl)methanone from Example 3 (580 mg, 2.02 mmol), and 3-amino-1H-pyrazole-5-carbonitrile (218 mg, 2.02 mmol) in DMF (5 mL) was stirred at rt overnight. MeOH (10 mL) was then added to this mixture, and the precipitate was filtered washed with MeOH, and dried to afford 3-(2-(4-fluorobenzoyl)quinazolin-4-ylamino)-1H-pyrazole-5-carbonitrile (170 mg, 23.4%) 1H NMR (300 MHz, DMSO-d6) δ 6.89 (s, 1H), 7.40 (d, 2H), 7.83 (s, 1H), 7.98 (m, 2H), 8.11 (m, 2H), 8.56 (s, 1H), 11.18 (s, 1H), 13.84 (s, 1H); LC-MS (ESI) m/z 359 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09308207B2
出典データセットuspto-grants-2016_04
ORD IDord-cbb08b6c34b540b68f2958c0c83cb07f
出典メモuspto-grants-2016_04