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4-Acetyl-2-butyl-5-cyano-1-tritylimidazole → HCID 178441657, 화합물

HRID 53021
노트
인쇄 미리보기

반응식

HRID 53021 반응식
[C:1]([C:4]1[N:5]=[C:6]([CH2:30][CH2:31][CH2:32][CH3:33])[N:7](C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[C:8]=1[C:9]#[N:10])(=[O:3])[CH3:2]>C(O)(=O)C>[C:1]([C:4]1[N:5]=[C:6]([CH2:30][CH2:31][CH2:32][CH3:33])[NH:7][C:8]=1[C:9]#[N:10])(=[O:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 190360854-Acetyl-2-butyl-5-cyano-1-tritylimidazole

생성물 1

HCID 178441657HCID 178441657, 화합물수율 84.1%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
60 °C

실험 절차

A suspension of 1.78 g of 4-acetyl-2-butyl-5-cyano-1-tritylimidazole [prepared as described in step (ii) above] in 80% v/v aqueous acetic acid was stirred at 60° C. for 1 hour. The solution thus obtained was concentrated to dryness by evaporation under reduced pressure. The resulting residue was purified by column chromatography through silica gel, using a 3:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.66 g of the title compound as a colorless solid, melting at 77°-78° C.

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  1. customThe solution thus obtained
  2. concentrationwas concentrated to dryness by evaporation under reduced pressure
  3. customThe resulting residue was purified by column chromatography through silica gel
  4. additionby volume mixture of hexane and ethyl acetate as the eluent

출처 및 근거

ORD 기록
ord-6e71515010dc416ea8566747e85dcd7a
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05616599

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