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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

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indazol-6-amineHCID 81423—
반응물DiisopropylethylamineHCID 81531—
반응물2,4-Dichloro-5-methyl-7-tosyl-7h-pyrrolo[2,3-d]pyrimidineHCID 58290852—
용매1-ButanolHCID 263—
용매Ethyl AcetateHCID 8857—
생성물2-Chloro-N-(1H-indazol-6-yl)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 8662803739.7%

반응 조건

온도90 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705004B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-05c1d9062c7f4ef0ab9e01e7fa29bed3
출처 메모uspto-grants-2010_04