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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 3,4,5-Trimethoxyphenyl isothiocyanate | HCID 118900 | — |
| 반응물 | Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate | HCID 11962077 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-6-carboxylate | HCID 11962078 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07501525B2 |
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| 출처 데이터셋 | uspto-grants-2009_03 |
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| ORD ID | ord-42067fc6e84247f4918deb5357125a06 |
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| 출처 메모 | uspto-grants-2009_03 |
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