참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | Thieno(2,3-b)pyridine | HCID 289928 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | Thieno[2,3-b]pyridine-3-sulfonyl chloride | HCID 18614041 | — |
반응 단계
A solution of thieno[2,3-b]pyridine (0.70 g, 5.2 mmoles), prepared as described in Example 1(A), in chlorosulfonic acid, (7 ml) was heated to 100° C. for 15 minutes, then cooled to ambient temperature and added to ice (100 ml). The pH of the aqueous phase as adjusted to 8 with sat. NaHCO3, then extracted with CHCl3 (2×125 ml). The organic phase was dried (MgSO4), filtered and concentrated to collect 0.95 g (78%) of the title compound as a tan solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06013655 |
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| 출처 데이터셋 | uspto-grants-2000_01 |
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| ORD ID | ord-09aca8f0d605409f8a1f64e8abed4ad1 |
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| 출처 메모 | uspto-grants-2000_01 |
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