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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4-Dichloroquinazoline | HCID 252886 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | Methyl 2-[4-(aminomethyl)phenyl]benzoate | HCID 1393434 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4'-[[(2-Chloro-4-quinazolinyl)amino]methyl][1,1'-biphenyl]-2-carboxylic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05256781 |
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| 出典データセット | uspto-grants-1993_10 |
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| ORD ID | ord-6cf6eac2bcc241f494fa89be5c9d0cdc |
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| 出典メモ | uspto-grants-1993_10 |
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