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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21044생성일: 2026년 10월 23일

3-Pyridinemethanamine → 4-Chloro-7-(1-(tert-butoxycarbonyl)-5-[(pyridin-3-ylmethyl)amino methyl]indol-2-yl)isoindolinone

https://huagongshe.com/ko/reaction/21044

반응식

참여 물질

역할이름HCID투입량
반응물3-PyridinemethanamineHCID 31018—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-Chloro-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinoneHCID 86628227—
용매DichloromethaneHCID 6344—
생성물4-Chloro-7-(1-(tert-butoxycarbonyl)-5-[(pyridin-3-ylmethyl)amino methyl]indol-2-yl)isoindolinoneHCID 68491978—

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 3-aminomethylpyridine (0.010 mL, 0.098 mmol) and sodium triacetoxyborohydride (32 mg, 0.15 mmol) to obtain 4-chloro-7-(1-(tert-butoxycarbonyl)-5-[(pyridin-3-ylmethyl)amino methyl]indol-2-yl)isoindolinone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5c7bc26dd9e049c4b0dceb6879ec458f
출처 메모uspto-grants-2010_06