참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclopentanol | HCID 7298 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylate | HCID 75557 | — |
| 반응물 | 1H-Indazol-5-ol | HCID 101438 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-(cyclopentyloxy)-1H-indazole | HCID 22933928 | 16% |
반응 단계
Cyclopentanol (0.068 ml, 0.745 mmol), triphenylphosphine (221 mg, 0.820 mmol) and dibenzyl azodicarboxylate (267 mg, 0.895 mmol) were added at 0° C. to a solution of the 1H-indazol-5-ol (100 mg, 0.745 mmol) obtained in Reference Example 4 in tetrahydrofuran (6 ml). After 30 minutes, the mixture thus obtained was heated to room temperature. After stirring overnight, the reaction solution was concentrated under reduced pressure and a 1M-aqueous sodium hydroxide solution (4 ml) and chloroform (3 ml) were added to the resulting residue. After removing the aqueous layer, water (2 ml) was added to the residue. The aqueous layer was removed and the organic layer was dried over anhydrous magnesium sulfate. The organic layer dried was concentrated and the resulting residue was purified by a silica gel column chromatography (eluent: chloroform/methanol, hexane/ethyl acetate) to obtain 5-(cyclopentyloxy)-1H-indazole (24 mg, 16%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07199147B2 |
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| 출처 데이터셋 | uspto-grants-2007_04 |
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| ORD ID | ord-7949bd9d092249aeaf3c59466e2055bd |
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| 출처 메모 | uspto-grants-2007_04 |
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