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Aluminum(III) Chloride → 4-(6-Hydroxyquinazolin-2-yl)benzoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Aluminum(III) Chloride | HCID 6451240 | — |
| 反応物 | 4-(6-Methoxyquinazolin-2-yl)benzoic acid | HCID 67974201 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(6-Hydroxyquinazolin-2-yl)benzoic acid | HCID 57407157 | 13% |
反応手順
To a suspension of 4-(6-methoxyquinazolin-2-yl)benzoic acid (220 mg, 0.785 mmol) in anhydrous CH2Cl2 (5 mL) was added AlCl3 (600 mg, 4.55 mmol), the reaction mixture was refluxed overnight. The mixture was quenched with sat.NH4Cl (10 mL), the aqueous layer was extracted with CH2Cl2/MeOH (v/v=10/1, 30 mL×3), the combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated to give the crude product, which purified by prep-HPLC (0.1% TFA as additive) to give Compound V-1 (27 mg, yield 13%). 1H NMR (MeOD 400 MHz): δ 9.42 (s, 1H), 8.60 (d, J=8.4 Hz, 2H), 8.17 (d, J=8.4 Hz, 2H), 8.00 (d, J=9.2 Hz, 1H), 7.60 (dd, J=9.2, 2.8 Hz, 1H), 7.30 (d, J=2.8 Hz, 1H). MS (ESI): m/z 266.9 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09221810B2 |
| 出典データセット | uspto-grants-2015_12 |
| ORD ID | ord-a5317a294b1b4778b26c94f22532aa29 |
| 出典メモ | uspto-grants-2015_12 |