돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1747357생성일: 2026년 10월 26일

Benzyltrimethylammonium hydroxide → 3-(3-1,2-Benzisoxazol-3-ylmethyl-2-oxo-2,3-dihydro-benzimidazol-1-yl)-hexanoic acid ethyl ester

https://huagongshe.com/reaction/1747357

반응식

참여 물질

역할이름HCID투입량
반응물Benzyltrimethylammonium hydroxideHCID 66854—
반응물Ethyl trans-2-hexenoateHCID 5364778—
반응물1-1,2-Benzisoxazol-3-ylmethyl-1,3-dihydro-benzimidazol-2-oneHCID 59497602—
용매DimethylformamideHCID 6228—
용매Ammonium ChlorideHCID 25517—
생성물3-(3-1,2-Benzisoxazol-3-ylmethyl-2-oxo-2,3-dihydro-benzimidazol-1-yl)-hexanoic acid ethyl esterHCID 5949731846%

반응 조건

온도60 °C

반응 단계

To a stirred solution of 1-1,2-benzisoxazol-3-ylmethyl-1,3-dihydro-benzimidazol-2-one (100 mg, 0.38 mmol) in DMF (5 ml) was added ethyl trans-2-hexenoate (80 mg, 0.57 mmol) followed by benzyltrimethylammonium hydroxide (Triton B, 40 wt % in MeOH, 17.0 ul). The resulting mixture was warmed to 60° C. for 12 h and cooled to ambient temperature. The reaction was diluted with NH4Cl (sat.) and the product was extracted into ethyl acetate (2×). The combined organics were dried (MgSO4), filtered and concentrated to give the crude product which was purified via column chromatography (silica gel, 5% EtOAc/dichloromethane). The product-containing fractions were combined and concentrated to give 70 mg (46%) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09150556B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-1f6ce19c6ca245a2bce6eeb1e70ff29f
출처 메모uspto-grants-2015_10