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HRID 1657173作成日:2026年10月26日

2,4-Dichloroquinazoline → 4'-[[(2-Chloro-4-quinazolinyl)amino]methyl][1,1'-biphenyl]-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1657173

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DichloroquinazolineHCID 252886—
反応物Sodium AcetateHCID 517045—
反応物Methyl 2-[4-(aminomethyl)phenyl]benzoateHCID 1393434—
溶媒TetrahydrofuranHCID 8028—
生成物4'-[[(2-Chloro-4-quinazolinyl)amino]methyl][1,1'-biphenyl]-2-carboxylic acid methyl esterHCID 15233818—

反応手順

Sodium acetate (0.65 g), 2,4-dichloroquinazoline (0.52 g) and 4'-aminomethyl[1,1'-biphenyl]-2-carboxylic acid methyl ester (0.73 g) were suspended in 25 mL of tetrahydrofuran. The reaction was stirred at room temperature for approximately 18 hours at which time the solvents were evaporated. The residue was loaded onto a silica gel column and the desired product was eluted with ethyl acetate/hexane (1:1). The yield was 0.75 g (71%) (m.p.=75°-90° C.): 1H NMR (DMSO-d6, 300 MHz) δ 9.30 (t, J=6 Hz, 1H), 8.33 (d, J=8.1 Hz, 1H), 7.81 (m, 1H), 7.71 (m, 1H), 7.60 (m, 3H), 7.45 (m, 4H), 7.25 (d, J=8.1 Hz, 2H), 4.80 (d, J=5.8 Hz, 2H), 3.58 (s, 3H); positive FAB MS m/e 404(MH). Anal. calcd for C23H18ClN3O2 : C, 68.40; H, 4.49; N,10.40. Found: C,68.09; H, 4.57; N, 10.10.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05256781
出典データセットuspto-grants-1993_10
ORD IDord-6cf6eac2bcc241f494fa89be5c9d0cdc
出典メモuspto-grants-1993_10