Methyl 4-Formylbenzoate → 4-(1-Ethyl-5-trifluoromethanesulfonyl-1H-benzoimidazol-2-yl)-benzoic acid methyl ester

HRID 1358761노트

반응식

HRID 1358761 반응식
[CH2:1]([NH:3][C:4]1[C:5]([NH2:17])=[CH:6][C:7]([S:10]([C:13]([F:16])([F:15])[F:14])(=[O:12])=[O:11])=[CH:8][CH:9]=1)[CH3:2].[CH:18]([C:20]1[CH:29]=[CH:28][C:23]([C:24]([O:26][CH3:27])=[O:25])=[CH:22][CH:21]=1)=O>C(O)CCCC>[CH3:27][O:26][C:24](=[O:25])[C:23]1[CH:28]=[CH:29][C:20]([C:18]2[N:3]([CH2:1][CH3:2])[C:4]3[CH:9]=[CH:8][C:7]([S:10]([C:13]([F:16])([F:14])[F:15])(=[O:11])=[O:12])=[CH:6][C:5]=3[N:17]=2)=[CH:21][CH:22]=1

참가 물질

4

반응물 2

HCID 15294Methyl 4-FormylbenzoateHCID 703518N1-ethyl-4-trifluoromethanesulfonylbenzene-1,2-diamine

생성물 1

HCID 99534764-(1-Ethyl-5-trifluoromethanesulfonyl-1H-benzoimidazol-2-yl)-benzoic acid methyl ester

시약·촉매·용매 1

HCID 62761-Pentanol용매

실험 절차

N1-Ethyl-4-trifluoromethanesulfonyl-benzene-1,2-diamine (134 mg, 0.50 mmol) and methyl 4-formylbenzoate (82 mg, 1.1 equiv) were dissolved in 0.8 mL dry pentanol and heated to reflux for 18 h. The reaction mixture was then evaporated to one-third volume by blowing with a stream of nitrogen while heating. Upon cooling, the solids were collected and washed with ether to yield 155 mg upon drying. The solids may be recrystallized from EtOAc/ether to yield pure ester 35: 1HNMR (400 MHz, d6-DMSO) δ 8.48 (d, J=1.65 Hz, 1H), 8.19 (m, 3H), 8.01 (m, 3H), 4.45 (q, J=7.24 Hz, 2H), 3.92 (s, 3H), 1.36 (t, J=7.22 Hz, 3H); LCMS-APCI in/z 413 [M+1]+.

후처리

  1. temperatureheated
  2. temperatureto reflux for 18 h
  3. customThe reaction mixture was then evaporated to one-third volume
  4. temperaturewhile heating
  5. temperatureUpon cooling
  6. customthe solids were collected
  7. washwashed with ether
  8. customto yield 155 mg
  9. customupon drying
  10. customThe solids may be recrystallized from EtOAc/ether

출처 및 근거

ORD 기록
ord-e80552a49e984ee0be17694fd5fb142c
출처 데이터셋
uspto-grants-2003_07
특허 번호
US06596772B1

반응 노트

불러오는 중…