Ethanethiol → 1-[[3-(Ethylthio)-2-pyrazinyl]oxy]-3-[(1-methylethyl)amino]-2-propanol
反応式
Cl[C:2]1[C:3]([O:8][CH2:9][CH:10]([OH:16])[CH2:11][NH:12][CH:13]([CH3:15])[CH3:14])=[N:4][CH:5]=[CH:6][N:7]=1.[CH2:17]([SH:19])[CH3:18].C[O-].[Na+]>CO>[CH2:17]([S:19][C:2]1[C:3]([O:8][CH2:9][CH:10]([OH:16])[CH2:11][NH:12][CH:13]([CH3:15])[CH3:14])=[N:4][CH:5]=[CH:6][N:7]=1)[CH3:18]参加物
5
実験手順
Analogously to the description in Example 8, 7.5 g (0.03 mol) of 3-chloro-2-(3'-isopropylamino-2'-hydroxy-propoxy)-pyrazine, 2.8 g (0.045 mol) of ethyl-mercaptan and 2.4 g (0.045 mol) of sodium methylate in 150 ml of methanol, when refluxed for 30 hours, give the crude base 3-ethylthio-2-(3'-isopropylamino-2'-hydroxypropoxy)-pyrazine, and this is converted, with 1.74 g of fumaric acid, into the fumarate of melting point 158°-160° C. when crystallised from methanol-ether.
出典と根拠
- ORDレコード
- ord-79b81bcca2e64becb29ea9d9e13f0260
- 出典データセット
- uspto-grants-1983_10
- 特許番号
- US04410530
反応ノート
読み込み中…