Ethyl Acetate → n-[2-[1-(3-Chloro-2-pyridinyl)-3-(trifluoromethyl)-1h-pyrazol-5-yl]-8-methyl-4h-3,1-benzoxazin-4-ylidene]-2-propanamine
반응식
[Cl:1][C:2]1[C:3]([N:8]2[C:12]([C:13]([NH:15][C:16]3[C:21]([C:22]([NH:24][CH:25]([CH3:27])[CH3:26])=[O:23])=[CH:20][CH:19]=[CH:18][C:17]=3[CH3:28])=O)=[CH:11][C:10]([C:29]([F:32])([F:31])[F:30])=[N:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1.C(OCC)(=O)C>P(Cl)(Cl)(Cl)=O>[Cl:1][C:2]1[C:3]([N:8]2[C:12]([C:13]3[O:23][C:22](=[N:24][CH:25]([CH3:27])[CH3:26])[C:21]4[CH:20]=[CH:19][CH:18]=[C:17]([CH3:28])[C:16]=4[N:15]=3)=[CH:11][C:10]([C:29]([F:30])([F:31])[F:32])=[N:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1참가 물질
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
A stirred solution of the title compound from Step D (1.2 g, 2.6 mmol) in 8 mL of phosphorous oxychloride was heated at reflux for 8 hours. The hot reaction solution was poured onto a large excess of ice and 100 ml of ethyl acetate added almost immediately (before allowing all of the ice to melt). After stirring and allowing the remaining ice to melt, the ethyl acetate layer was separated, washed with water, aqueous saturated sodium bicarbonate and brine. Followed by drying over magnesium sulfate, the solvent was removed in vacuo to give a crude yellow oily solid residue. Purification by flash chromatography on silica gel (4:1 hexane/ethyl acetate as eluant) afforded 450 mg of the title compound, a compound of the invention, isolated as a white solid melting at 175–176° C.
후처리
- temperatureat reflux for 8 hours
- additionadded almost immediately (
- customthe ethyl acetate layer was separated
- washwashed with water, aqueous saturated sodium bicarbonate and brine
- dry with materialFollowed by drying over magnesium sulfate
- customthe solvent was removed in vacuo
- customto give a crude yellow oily solid residue
- customPurification by flash chromatography on silica gel (4:1 hexane/ethyl acetate as eluant)
출처 및 근거
- ORD 기록
- ord-e9da73c7500c4e01954614202bb2d8c0
- 출처 데이터셋
- uspto-grants-2006_12
- 특허 번호
- US07148217B2
반응 노트
불러오는 중…