HCID 12841761、化合物 → 3-beta-(4-Carbamoylmethoxyphenylacetamido)ethylamino-1-(2-cyanophenoxy)-2-propanol
反応式
[NH2:1][CH2:2][CH2:3][NH:4][CH2:5][CH:6]([OH:17])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]#[N:16].[C:18]([CH2:21][O:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][C:30](OCC)=[O:31])=[CH:25][CH:24]=1)(=[O:20])[NH2:19]>>[C:18]([CH2:21][O:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][C:30]([NH:1][CH2:2][CH2:3][NH:4][CH2:5][CH:6]([OH:17])[CH2:7][O:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]#[N:16])=[O:31])=[CH:25][CH:24]=1)(=[O:20])[NH2:19]参加物
3
実験手順
In a similar manner using 2.36 g. of 3-(β-aminoethylamino)-1-(2-cyanophenoxy)-2-propanol and 2.37 g. of ethyl 4-carbamoylmethoxyphenylacetate as starting materials there is obtained 3-β-(4-carbamoylmethoxyphenylacetamido)ethylamino-1-(2-cyanophenoxy)-2-propanol, isolated as its hydrogen oxalate, m.p. 123°-125° C. after crystallisation from ethyl acetate.
出典と根拠
- ORDレコード
- ord-d73615f25c794710b95c2d54a91c518e
- 出典データセット
- uspto-grants-1979_02
- 特許番号
- US04141987
反応ノート
読み込み中…