HCID 66936015、化合物 → (4Ar,8as)-1-methyldecahydroquinoxaline
反応式
[CH3:1][N:2]1[C@@H:11]2[C@@H:6]([CH2:7][CH2:8][CH2:9][CH2:10]2)[N:5](C(OCC2C=CC=CC=2)=O)[CH2:4][CH2:3]1>CO>[CH3:1][N:2]1[C@@H:11]2[C@@H:6]([CH2:7][CH2:8][CH2:9][CH2:10]2)[NH:5][CH2:4][CH2:3]1参加物
3
実験手順
Phenylmethyl (4aS,8aR)-4-methyloctahydro-1(2H)-quinoxalinecarboxylate (2.7 g, 9.4 mmol) was dissolved in 140 mL of MeOH, degassed and placed under argon. 10% Pd/C (400 mg) was added, and the contents were thoroughly degassed and placed under a hydrogen balloon for approximately 2 hrs. The contents were then degassed and filtered through Celite, and the Celite pad was washed with DCM and MeOH. After 19.6 mL 1N HCl was added, the resulting filtrate was concentrated in vacuo to provide the hydrochloride salt of (4aR,8aS)-1-methyldecahydroquinoxaline (2.1 g, 100%). LCMS: (M+H)+: 155.1.
後処理
- customdegassed
- addition10% Pd/C (400 mg) was added
- customthe contents were thoroughly degassed
- customfor approximately 2 hrs
- customThe contents were then degassed
- filtrationfiltered through Celite
- washthe Celite pad was washed with DCM and MeOH
- additionAfter 19.6 mL 1N HCl was added
- concentrationthe resulting filtrate was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-2207c62860274943abe7e9e2ad90d50e
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07893056B2
反応ノート
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