Isopropenyl acetate → 1-(7-Amino-3,4-dihydroisoquinolin-2(1H)-yl)ethan-1-one
反応式
[NH2:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][NH:8][CH2:9]2)=[CH:4][CH:3]=1.[C:12](OC(C)=C)(=[O:14])[CH3:13]>C(OCC)(=O)C>[C:12]([N:8]1[CH2:7][CH2:6][C:5]2[C:10](=[CH:11][C:2]([NH2:1])=[CH:3][CH:4]=2)[CH2:9]1)(=[O:14])[CH3:13]参加物
4
実験手順
A mixture of 2.5 g. (16.8 mmol) 7-amino-1,2,3,4-tetrahydroisoquinoline, 30 ml. ethyl acetate and 2 ml. isopropenyl acetate was refluxed for approximately 16 hours and was then concentrated to dryness at reduced pressure. The residue was then recrystallized from a mixture of ethyl acetate and petroleum ether to afford 2-acetyl-7-amino-1,2,3,4-tetrahydroisoquinoline with a melting point of 98°-100° C.
後処理
- additionA mixture of 2.5 g
- concentrationwas then concentrated to dryness at reduced pressure
- customThe residue was then recrystallized from a mixture of ethyl acetate and petroleum ether
出典と根拠
- ORDレコード
- ord-85e629680283409ea9fc1a6d928d5202
- 出典データセット
- uspto-grants-1982_03
- 特許番号
- US04321254
反応ノート
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