4-Methylmorpholine → N-methoxy-N-methyl-2-propylamino-4-trifluoromethyl-benzamide
반응식
[CH2:1]([NH:4][C:5]1[CH:13]=[C:12]([C:14]([F:17])([F:16])[F:15])[CH:11]=[CH:10][C:6]=1[C:7](O)=[O:8])[CH2:2][CH3:3].[CH3:18][NH:19][O:20][CH3:21].CN1CCOCC1.C[N+]1(C2N=C(OC)N=C(OC)N=2)CCOCC1.[Cl-]>C(Cl)Cl>[CH3:21][O:20][N:19]([CH3:18])[C:7](=[O:8])[C:6]1[CH:10]=[CH:11][C:12]([C:14]([F:17])([F:16])[F:15])=[CH:13][C:5]=1[NH:4][CH2:1][CH2:2][CH3:3]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
2-Propylamino-4-(trifluoromethyl)benzoic acid (147 mg, 0.594 mmol) in CH2Cl2 was reacted with N,O-dimethylhydroxy amine (82 mg), NMM (0.2 ml) and DMTMM (222 mg) at room temperature overnight. The reaction mixture was quenched by adding H2O (3 ml). The reaction solvent was removed under reduced pressure. Water (30 ml) was added to the resulting residue, which was extracted with ethylacetate (30 ml×3). The combined organic layer was washed with sat. NaHCO3 solution (30 ml), 1N HCl aqueous solution (30 ml) and brine (30 ml), and then dried over MgSO4. The filterate was concentrated in vacuo. The residue was purified with column chromatography to yield the title compound (98 mg, 57%).
후처리
- customThe reaction mixture was quenched
- additionby adding H2O (3 ml)
- customThe reaction solvent was removed under reduced pressure
- additionWater (30 ml) was added to the resulting residue, which
- extractionwas extracted with ethylacetate (30 ml×3)
- washThe combined organic layer was washed with sat. NaHCO3 solution (30 ml), 1N HCl aqueous solution (30 ml) and brine (30 ml)
- dry with materialdried over MgSO4
- concentrationThe filterate was concentrated in vacuo
- customThe residue was purified with column chromatography
출처 및 근거
- ORD 기록
- ord-27f52a2ac0454ec19f032603d79107da
- 출처 데이터셋
- uspto-grants-2013_10
- 특허 번호
- US08557872B2
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