참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Methylfuran | HCID 10797 | — |
| 반응물 | N-(5-bromothiophenesulfonyl)pyrrole | HCID 23445587 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 촉매 | Zincchloride | HCID 3007855 | — |
| 촉매 | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole | HCID 22998481 | 19.3% |
반응 단계
t-BuLi (1.7 m solution in hexane, 7.9 ml, 14.6 mmol) was added dropwise under constant stirring under a nitrogen atmosphere to a solution of 2-methylfuran (1.0 g, 12 mmol) in THF (20 ml) at -78° C. The solution was then warmed to -10° C. and stirring continued for 45 min. The solution was then added to a solution of zinc chloride (27 ml of a 0.5M solution in THF) at -30° C. and then warmed to room temperature where stirring continued for 1 hr. resulting in a pale yellow clear solution. The solution was then transferred via a steel canula under nitrogen to a solution of N-(5-bromothiophene-2-sulfonyl)pyrrole (Example 33A, 3.5 g, 12 mmol) and tetrakis(triphenylphosphine)-palladium (0) (693 mg, 0.6 mmol) in THF (15 ml) at -78° C. The solution was then warmed to room temperature and stirred for a period of 2 hours. Purification by column chromatography using 2% ethyl acetate gave 680 mg of N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole as a pale yellow powder (19% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05594021 |
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| 출처 데이터셋 | uspto-grants-1997_01 |
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| ORD ID | ord-bcaac69dab8048f9bc83dbb0247428f4 |
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| 출처 메모 | uspto-grants-1997_01 |
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