反応式
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][C:2]1=[O:10].[C:11](OCI)(=O)C(C)(C)C.[OH:20][C:21]1[CH:26]=[CH:25][C:24]([CH:27]([C:33]#[C:34][CH3:35])[CH2:28][C:29]([O:31]C)=[O:30])=[CH:23][CH:22]=1>>[O:10]=[C:2]1[N:3]([CH2:11][O:20][C:21]2[CH:26]=[CH:25][C:24]([CH:27]([C:33]#[C:34][CH3:35])[CH2:28][C:29]([OH:31])=[O:30])=[CH:23][CH:22]=2)[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[S:1]1参加物
4
実験手順
Analogously to example 6, 3H-benzothiazol-2-one, iodomethyl pivalate and methyl 3-(4-hydroxyphenyl)hex-4-ynoate were used to obtain 3-[4-(2-oxobenzothiazol-3-ylmethoxy)-phenyl]hex-4-ynoic acid.
出典と根拠
- ORDレコード
- ord-9dce468465bd408db8044e09cd781334
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08530413B2
関連ノート
読み込み中…