反応式
[CH2:1]1[CH:9]2[CH:4]([CH:5]3[CH2:10][CH:8]2[CH2:7][CH:6]3[NH2:11])[CH:3]=[CH:2]1.C1C2C(C3CC2CC3N)CC=1>CO.[Pd]>[CH2:1]1[CH:9]2[CH:4]([CH:5]3[CH2:10][CH:8]2[CH2:7][CH:6]3[NH2:11])[CH2:3][CH2:2]1参加物
5
実験手順
3.3 g of a mixture of 3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-5-ylamine and 3a,4,5,6,7,7a-hexahydro-3H-4,7-methanoinden-5-ylamine (example Amine 1, a2) were dissolved in 30 ml of methanol and reduced under an atmosphere of hydrogen in the presence of 0.5 g Pd/C (10%). After 4 hours the catalyst was filtered off and washed with methanol. The filtrate was concentrated in vaccuo to give 3 g of the desired product as an oil.
後処理
- filtrationAfter 4 hours the catalyst was filtered off
- washwashed with methanol
- concentrationThe filtrate was concentrated in vaccuo
出典と根拠
- ORDレコード
- ord-1284b9f2c39a427889a947f298a8e931
- 出典データセット
- uspto-grants-2004_11
- 特許番号
- US06825231B2
関連ノート
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