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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1727415생성일: 2026년 10월 27일

Diisopropylcarbodiimide → methyl-2-[(3,5-dimethoxyphenyl)amino]-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-1H-benzimidazole-5-carboxylate

https://huagongshe.com/reaction/1727415

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물3,5-Dimethoxyphenyl isothiocyanateHCID 145422—
반응물Methyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoateHCID 69027376—
용매TetrahydrofuranHCID 8028—
생성물methyl-2-[(3,5-dimethoxyphenyl)amino]-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-1H-benzimidazole-5-carboxylateHCID 6902764276%

반응 단계

3,5 dimethoxyphenylisothiocyanate (571 mg, 1 eq) and diisopropylcarbodiimide (1.35 ml, 4 eq) are added successively to a solution of methyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoate (1.0 g, 1 eq) in tetrahydrofuran (10 ml). The mixture is heated under reflux for 18 hours then cooled down to ambient temperature and concentrated under reduced pressure at 40° C. The residue is taken up in ethyl acetate (100 ml) and water (40 ml). After decanting and extracting, the combined organic phases are washed with salt water, dried over Na2SO4 then evaporated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent: dichloromethane/methanol 99:1 to 98:2) produces the expected compound in the form of a beige foam (1.12 g; 76% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07495110B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-f1e39c8788fd45f9ac45d27ca0a27676
출처 메모uspto-grants-2009_02