関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Lithium hydroxide, monohydrate | HCID 168937 | — |
| 反応物 | 4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid | HCID 21991771 | — |
| 反応物 | 4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester | HCID 69594337 | — |
| 反応物 | 4-(3-Fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester | HCID 86593646 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide | HCID 10020180 | 65% |
反応手順
4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid: A mixture of 4-(3-fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester (14.0 g, 35.0 mmol) in THF (120 mL) and water (120 mL), containing lithium hydroxide monohydrate (2.94 g, 70.1 mmol) was stirred at rt for 48 h. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and then the mixture extracted with diethyl ether (3×150 mL). The aqueous phase was then adjusted to pH 2 with HCl. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and the aqueous phase was then adjusted to pH 5.2 with HCl then the mixture extracted with diethyl ether (3×100 mL). The combined extracts were then washed with brine (100 mL) dried and evaporated to afford title compound (6.6 g, 65%) as a light yellow solid. MS: m/e=290.0 (M−H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07087612B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-ad3689421b0444ecba177dceb56a6917 |
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| 出典メモ | uspto-grants-2006_08 |
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