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HRID 2188583作成日:2026年10月24日
1,3-Benzodioxole-5-carbonyl chloride → Benzo[1,3]dioxole-5-carboxylic acid (4-{3-[2-(3-trifluoromethyl-benzoylamino)-acetylamino]-azetidin-1-yl}-cyclohexyl)-amide
https://huagongshe.com/ja/reaction/2188583
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1,3-Benzodioxole-5-carbonyl chloride | HCID 2734749 | — |
| 反応物 | N-{[1-(4-Amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide TFA salt | HCID 86646662 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Benzo[1,3]dioxole-5-carboxylic acid (4-{3-[2-(3-trifluoromethyl-benzoylamino)-acetylamino]-azetidin-1-yl}-cyclohexyl)-amide | HCID 49763337 | — |
反応手順
Benzo[1,3]dioxole-5-carbonyl chloride (Aldrich, 74 mg, 0.404 mmol) was added into a solution of N-{[1-(4-amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide TFA salt (as prepared in the previous step 200 mg, 0.404 mmol) and TEA (170 μL, 1.21 mmol) in DCM (5 mL) at 0° C. The reaction was stirred for an additional 2 hours and quenched with saturated sodium bicarbonate. The reaction was then partitioned between DCM and water. The organic layer was separated and the aqueous layer was extracted 3 times with a chloroform/IPA “cocktail” (˜3:1, v/v). The combined organic layer was dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was then purified by a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford the title compound as white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08324186B2 |
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| 出典データセット | uspto-grants-2012_12 |
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| ORD ID | ord-96d423cb081e4ff3b151feca3af765ac |
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| 出典メモ | uspto-grants-2012_12 |
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