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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1784300생성일: 2026년 10월 25일

Diisopropylcarbodiimide → methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-6-carboxylate

https://huagongshe.com/reaction/1784300

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물3,4,5-Trimethoxyphenyl isothiocyanateHCID 118900—
반응물Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoateHCID 11962077—
용매TetrahydrofuranHCID 8028—
생성물methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-6-carboxylateHCID 1196207836%

반응 단계

3,4,5-trimethoxyphenyl isothiocyanate (6.6 g, 1.2 eq) and diisopropylcarbodiimide (9.1 g, 3 eq) are successively added to a solution of methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate (7.75 g, 1 eq) in tetrahydrofuran (130 ml). The mixture is heated under reflux for 16 hours then cooled down to ambient temperature and concentrated under reduced pressure at 40° C. Water (100 ml) and dichloromethane (200 ml) are added to the residue obtained. After decantation and extractions, the combined organic phases are washed with salt water, dried over Na2SO4 then concentrated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent:heptane/ethyl acetate 8:2 to 3:7) produces the expected compound in the form of a solid which is washed with ether. (4.4 g; 36% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07501525B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-42067fc6e84247f4918deb5357125a06
출처 메모uspto-grants-2009_03