Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1747328생성일: 2026년 10월 26일
Methanol → 3-[3-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester
https://huagongshe.com/reaction/1747328
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| 반응물 | Ethyl trans-2-hexenoate | HCID 5364778 | — |
| 반응물 | 1-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-one | HCID 59497379 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-[3-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester | HCID 59497617 | 95% |
반응 단계
To a solution of 1-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-one (50 mg, 0.17 mmol) in dry DMF (1.0 mL) are added (E)-Hex-2-enoic acid ethyl ester (27 mg, 0.19 mmol) and 40% benzyltrimethyl ammonium hydroxide in MeOH (0.008 mL, 0.017 mmol). The resulting mixture is warmed up to 60° C. for 16 hr. Then another 27 mg of (E)-Hex-2-enoic acid ethyl ester is added the heating is continued for another 8 hr. Then saturated NH4Cl (2 mL) and water (10 mL) are added and the mixture is extracted with EtOAc (3×25 mL). The organic layers are combined, dried over MgSO4 and concentrated to give the crude product. Purification with flash column chromatography using 20% EtOAc in Hexanes affords 70 mg (95%) of 3-[3-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09150556B2 |
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| 출처 데이터셋 | uspto-grants-2015_10 |
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| ORD ID | ord-73fcba765c7348dc976c9e08883714bf |
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| 출처 메모 | uspto-grants-2015_10 |
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