反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.CN(C=O)C.C(Cl)(=O)C(Cl)=O.[CH:23]1([NH2:26])[CH2:25][CH2:24]1.CCN(C(C)C)C(C)C>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([NH:26][CH:23]1[CH2:25][CH2:24]1)=[O:9]参加物
反応条件
- 温度
- 0 °C
実験手順
To a toluene solution (1 M) of 5-chloro-2-methylbenzoic acid (1 eq.) and DMF (1.2 eq.) was added at 0° C. oxalyl chloride (1.2 eq.) dropwise over 1 h. The resulting solution was stirred at 0° C. for 2 h before the volatiles were removed in vacuo. The resulting residue was taken up in dichloromethane (1 M), cooled to 0° C. and added sequentially cyclopropylamine (1.5 eq.) and Hunig's base (2 eq.) dropwise. The resulting suspension was stirred at RT for 18 h. The reaction was quenched with 1 N aq. HCl and extracted with dichloromethane. The combined organic extracts were dried over MgSO4, filtered and the filtrate concentrated in vacuo to ˜1/3 in volume. The resulting white suspension was added an equivalent volume of hexanes and the title compound was isolated via vacuum filtration.
後処理
- customwere removed in vacuo
- temperaturecooled to 0° C.
- stirringThe resulting suspension was stirred at RT for 18 h
- customThe reaction was quenched with 1 N aq. HCl
- extractionextracted with dichloromethane
- dry with materialThe combined organic extracts were dried over MgSO4
- filtrationfiltered
- concentrationthe filtrate concentrated in vacuo to ˜1/3 in volume
- additionThe resulting white suspension was added an equivalent volume of hexanes
出典と根拠
- ORDレコード
- ord-4cb72e21895442acac8909515f40dfce
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889714B2
関連ノート
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