참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 4-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-B]pyridine | HCID 45074561 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine | HCID 46907955 | — |
반응 단계
To a −78° C. solution of Example 135A (250 mg, 0.741 mmol) in 10 mL tetrahydrofuran was added lithium diisopropylamide (2.0M solution in tetrahydrofuran, 0.556 mL, 1.112 mmol) slowly over the course of 5 minutes. The resulting solution was stirred at the same temperature for 30 minutes after which iodine (376 mg, 1.483 mmol) in 5 mL of tetrahydrofuran was slowly added over 10 minutes. The reaction was stirred at −78° C. for 2.5 hours, and was quenched by addition of 1M aqueous sodium thiosulfate solution. The mixture was extracted with dichloromethane. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated to give the title compound. MS (ESI+) m/z 462 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09328112B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-18091cced3024011912f07ec0df5ca20 |
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| 출처 메모 | uspto-grants-2016_05 |
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