反応式
Cl.[CH3:2][NH:3][CH:4]1[CH2:9][CH2:8][O:7][CH2:6][CH2:5]1.FC(F)(F)S([O-])(=O)=O.[N:18]1([S:23](N2C=C[NH+](C)C2)(=[O:25])=[O:24])[CH:22]=[CH:21][N:20]=[CH:19]1>>[CH3:2][N:3]([CH:4]1[CH2:9][CH2:8][O:7][CH2:6][CH2:5]1)[S:23]([N:18]1[CH:22]=[CH:21][N:20]=[CH:19]1)(=[O:25])=[O:24]参加物
3
実験手順
Imidazole-1-sulfonic acid methyl-(tetrahydro-pyran-4-yl)-amide was prepared in accordance with step A of the general method described in example 76 from methyl-(tetrahydro-pyran-4-yl)amine hydrochloride and 3-(1H-imidazol-1-ylsulfonyl)-1-methyl-1H-imidazolium trifluoromethanesulfonate; MS: m/e=246.8 (M+H+).
出典と根拠
- ORDレコード
- ord-b6ee7d822a374602895fe005c5cdeea1
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08183380B2
関連ノート
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