돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251205생성일: 2026년 10월 26일

1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanal → 2-{4-[[1-(3-Methyl-pyridin-2-yl)-ethyl]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-butyl}-isoindole-1,3-dione

https://huagongshe.com/reaction/251205

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanalHCID 77150—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(3-Methylpyridin-2-yl)ethan-1-amineHCID 45791166—
용매DichloromethaneHCID 6344—
용매Sodium BicarbonateHCID 516892—
생성물2-{4-[[1-(3-Methyl-pyridin-2-yl)-ethyl]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-butyl}-isoindole-1,3-dioneHCID 67272522—

반응 단계

To a solution of the above amine and 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyraldehyde (127 mg, 0.58 mmol) in CH2Cl2 (2.5 mL) was added NaBH(OAc)3 (117 mg, 0.55 mmol) and the reaction was stirred at room temperature under N2 for 16 hours. The mixture was diluted with saturated aqueous NaHCO3 (10 mL) and was extracted with CH2Cl2 (10 mL×3). The combined organic solution was dried (MgSO4), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (CH2Cl2/MeOH, 9:1) gave 2-{4-[[1-(3-methyl-pyridin-2-yl)-ethyl]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-butyl}-isoindole-1,3-dione as a 1:1 mixture of two diastereomers (72 mg, 0.15 mmol, 43%) along with some single diastereomer (33 mg, 0.07 mmol, 20%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863293B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-f0f15f6ef15d4b0cb2055b86bf23ad42
출처 메모uspto-grants-2011_01