反応式
Cl[C:2]1[N:7]=[C:6]([Cl:8])[N:5]=[C:4]([O:9][CH3:10])[N:3]=1.CCN(C(C)C)C(C)C.[F:20][CH:21]([F:32])[O:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][NH2:31])=[CH:25][CH:24]=1.CCOC(C)=O>C(#N)C.O>[Cl:8][C:6]1[N:5]=[C:4]([O:9][CH3:10])[N:3]=[C:2]([NH:31][CH2:30][CH2:29][C:26]2[CH:25]=[CH:24][C:23]([O:22][CH:21]([F:20])[F:32])=[CH:28][CH:27]=2)[N:7]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 1.8 g of 2,4-dichloro-6-methoxy-1,3,5-triazine in 40 ml of acetonitrile is cooled on an ice bath, 1.28 ml of DIPEA and then 1.68 g of 2-[4-(difluoromethoxy)phenyl]ethanamine are added and the mixture is stirred for 30 minutes. The reaction mixture is diluted by adding 100 ml of EtOAc and 50 ml of water, the phases are separated by settling, the organic phase is washed with saturated NaCl solution and dried over MgSO4, and the solvent is evaporated off under vacuum. The residue is taken up in DCM, the insoluble matter is filtered off and the filtrate is concentrated under vacuum. The residue is chromatographed on silica gel, eluting with a cyclohexane/EtOAc mixture in a gradient of from (95/5 v/v) to (80/20 v/v). 0.94 g of the expected compound is obtained.
後処理
- additionThe reaction mixture is diluted
- customthe phases are separated
- washthe organic phase is washed with saturated NaCl solution
- dry with materialdried over MgSO4
- customthe solvent is evaporated off under vacuum
- filtrationthe insoluble matter is filtered off
- concentrationthe filtrate is concentrated under vacuum
- customThe residue is chromatographed on silica gel
- washeluting with a cyclohexane/EtOAc mixture in a gradient of from (95/5 v/v) to (80/20 v/v)
出典と根拠
- ORDレコード
- ord-b9beb49da07947d8883b89d17e513bab
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09115121B2
関連ノート
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