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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21060생성일: 2026년 10월 24일

1-(2-Pyrimidinyl)piperazine → 4-Chloro-7-(1-(tert-butoxycarbonyl)-5-[4-(pyrimidin-2-yl)piperazin-1-ylmethyl]indol-2-yl)isoindolinone

https://huagongshe.com/ko/reaction/21060

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Pyrimidinyl)piperazineHCID 88747—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-Chloro-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinoneHCID 86628227—
용매DichloromethaneHCID 6344—
생성물4-Chloro-7-(1-(tert-butoxycarbonyl)-5-[4-(pyrimidin-2-yl)piperazin-1-ylmethyl]indol-2-yl)isoindolinoneHCID 68491662—

반응 단계

In a similar manner to Step 1 of Example 56, 4-chloro-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone (20.0 mg, 0.0487 mmol) was dissolved in dichloromethane (0.5 mL). The solution was treated with 1-(2-pyrimidyl)piperazine (33 mg, 0.20 mmol) and sodium triacetoxyborohydride (32 mg, 0.15 mmol) to obtain 4-chloro-7-(1-(tert-butoxycarbonyl)-5-[4-(pyrimidin-2-yl)piperazin-1-ylmethyl]indol-2-yl)isoindolinone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-44ad9a8143d54eb9950b96aa145e691b
출처 메모uspto-grants-2010_06