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HRID 77380作成日:2026年10月25日
Lithium Hydroxide → 2-(6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-ethyl-4-oxoquinazolin-3(4H)-yl)acetic acid
https://huagongshe.com/reaction/77380
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Lithium Hydroxide | HCID 3939 | — |
| 反応物 | Ethyl orthopropionate | HCID 66995 | — |
| 反応物 | 2-(2-Amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)benzamido)acetic acid | HCID 67114714 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-(6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-ethyl-4-oxoquinazolin-3(4H)-yl)acetic acid | HCID 69928597 | — |
反応手順
2-(2-Amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)benzamido)acetic acid (85.3 mg, 0.27 mmol) (Intermediate 9A) (100 mg, 0.36 mmol) was dissolved in triethoxypropane (1 mL), and heated in the microwave at 160° C. for 10 minutes. Reaction allowed to cool to room temperature and lithium hydroxide solution added (0.5 mL, 1M in methanol) and reaction stirred overnight. Organic layer purified using a 1 g SCX cartridge, followed by preparative-HPLC. Purified sample was free-based using 500 mg SCX cartridge to afford 2-(6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-ethyl-4-oxoquinazolin-3(4H)-yl)acetic acid (76 mg, 0.21 mmol).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08841289B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-8084490e27de4145b90648157fce16ca |
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| 出典メモ | uspto-grants-2014_09 |
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