関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| 反応物 | Di-tert-butyl dicarbonate | HCID 90495 | — |
| 反応物 | Tert-butyl 3-iodo-5-(n-tert-butoxycarbonyl-2-thiophenesulfonylamino)indazolecarboxylate | HCID 22567122 | — |
| 反応物 | HCID 178507363 | HCID 178507363 | — |
| 生成物 | {n-[3-(1h-Indol-2-yl)-1h-indazol-5-yl]}thiophene-2-sulfonamide | HCID 135855049 | — |
反応手順
tert-Butyl 3-iodo-5-(N-tert-butoxycarbonyl-2-thiophenesulfonylamino)-indazolecarboxylate can be prepared as described in Example 85 using 2 g of 5-amino-3-iodo-1H-indazole and 1.61 g of thiophene-2-sulfonyl chloride. The intermediate crude is purified by flash chromatography (98/2 by volume dichloromethane/methanol), resulting in 2.30 g of an orangey solid, which is then treated with 3.71 g of di-tert-butyl dicarbonate according to the procedure. After purification by flash chromatography (eluent:dichloromethane), 3.15 g of tert-butyl 3-iodo-5-(N-tert-butoxycarbonyl-2-thiophenesulfonylamino)indazolecarboxylate are obtained in the form of a white solid melting at 163° C. (LC/MS analysis: Tr=4.34 minutes; [M+H]+=605.93; [M+H]+-tert-butyl=549.90).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06858638B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-eb485f0229fc4601a63bfa1f3a95ed9d |
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| 出典メモ | uspto-grants-2005_02 |
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