Toluene → HCID 23134773, 화합물
반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6].Br[CH2:14][C:15]1[CH:20]=[CH:19][C:18]([C:21](=[O:26])[C:22]([O:24][CH3:25])=[O:23])=[CH:17][CH:16]=1.C(N(C(C)C)CC)(C)C.C1(C)C=CC=CC=1>O1CCOCC1>[CH2:8]([O:7][C:5]([C:4]1[CH:3]=[C:2]([NH:1][CH2:14][C:15]2[CH:16]=[CH:17][C:18]([C:21](=[O:26])[C:22]([O:24][CH3:25])=[O:23])=[CH:19][CH:20]=2)[CH:12]=[CH:11][CH:10]=1)=[O:6])[CH3:9]참가 물질
반응 조건
- 온도
- 60 °C
실험 절차
To a solution of ethyl 3-aminobenzoate (7.3 ml) and methyl 2-[4-(bromomethyl)phenyl]-2-oxoacetate (6.4 g) in dioxane (40 ml) was added diisopropylethylamine (6.4 ml), and the mixture was stirred at 60° C. for 2 hrs. The mixture was allowed to return to room temperature and toluene (330 ml) was added. The mixture was left standing at 0° C. for 5 hrs and the precipitated diisopropylethylamine hydrobromide was filtered off. The filtrate was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate and water. The ethyl acetate layer was separated, washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (hexane-ethyl acetate:4-1 v/v) to give the object compound (7.61 g) as a syrup.
후처리
- customto return to room temperature
- waitThe mixture was left
- waitstanding at 0° C. for 5 hrs
- filtrationthe precipitated diisopropylethylamine hydrobromide was filtered off
- concentrationThe filtrate was concentrated under reduced pressure
- dissolutionthe residue was dissolved in ethyl acetate
- customThe ethyl acetate layer was separated
- washwashed with water
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-3c4107cb7271420eafae2ff9ee63e833
- 출처 데이터셋
- uspto-grants-2008_08
- 특허 번호
- US07417052B2
반응 노트
불러오는 중…