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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

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Ammonium ChlorideHCID 25517—
반응물Benzyltrimethylammonium hydroxideHCID 66854—
반응물Ethyl trans-2-hexenoateHCID 5364778—
반응물1-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-oneHCID 59497379—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-[3-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl esterHCID 5949761795%

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09150556B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-73fcba765c7348dc976c9e08883714bf
출처 메모uspto-grants-2015_10