Benzyl(cyclopropylmethyl)amine → Cyclopropyl-(tetrahydro-pyran-3-ylmethyl)-carbamoyl chloride
反応式
[CH2:1]([N:8]([CH:12]1[CH2:14][CH2:13]1)[C:9]([Cl:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=C[CH:3]=1.C1(NCC2CCC[O:22]C2)CC1.C(NCC1CC1)C1C=CC=CC=1>C(Cl)Cl.CO>[CH:12]1([N:8]([CH2:1][CH:2]2[CH2:7][CH2:6][CH2:5][O:22][CH2:3]2)[C:9]([Cl:11])=[O:10])[CH2:14][CH2:13]1参加物
5
実験手順
The title compound is prepared analogously as described for benzyl-cyclopropyl-carbamoyl chloride starting from cyclopropyl-(tetrahydro-pyran-3-ylmethyl)-amine (prepared analogously as described for benzyl-cyclopropylmethyl-amine). TLC, Rf (CH2Cl2/MeOH 95:5)=0.9.
後処理
- customprepared analogously
出典と根拠
- ORDレコード
- ord-c2c07643084041728ce1025edf36a2e9
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07807709B2
反応ノート
読み込み中…