Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645695생성일: 2026년 10월 25일
1H-Indazol-6-amine → 2-Chloro-N-(1H-indazol-6-yl)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine
https://huagongshe.com/reaction/645695
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1H-Indazol-6-amine | HCID 81423 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2,4-Dichloro-5-methyl-7-tosyl-7h-pyrrolo[2,3-d]pyrimidine | HCID 58290852 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-Chloro-N-(1H-indazol-6-yl)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 86628037 | 39.7% |
반응 단계
To a solution of 2,4-dichloro-5-methyl-7-tosyl-pyrrolo[2,3-d]pyrimidine (0.36 g, 1 mmol) in n-butyl alcohol (3 mL) was added 6-aminoindazole (0.27 g, 2 mmol) and DIPEA (0.27 mL, 1.5 mmol) at room temperature. After heating at 90° C. for 4 h, the mixture was diluted with ethylacetate and the organic layer was sequentially washed with 1N HCl, saturated NaHCO3, and brine. The organic extract was then dried over Na2SO4 and concentrated to give a crude residue, which was purified by flash column (Hex/EtOAc=1:1) to give 2-Chloro-N-(1H-indazol-6-yl)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.18 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07705004B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-05c1d9062c7f4ef0ab9e01e7fa29bed3 |
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| 출처 메모 | uspto-grants-2010_04 |
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