Indole → Tryptamine
反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[NH4+:10].[Cl-].C(Cl)(Cl)Cl.Cl[CH:17](Cl)[CH3:18]>>[NH2:10][CH2:17][CH2:18][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1参加物
5
実験手順
To a solution of (S)-4b (30 mg) in dichloroethane (1 mL) cooled at −5° C. was dropwise added AgClO4. The resulting mixture was stirred for 15 min at the same temperature and added to a solution of indole (50 mg) in dichloroethane (1 mL) warmed in a reaction flask. The reaction mixture was stirred for 10 h at 50° C. and treated with saturated NH4Cl (mL), and extracted with CH2Cl2. The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo to the dryness. The residue was purified by silica gel (60-230 mesh) column chromatography eluted with 10% ethyl acetate in hexanes to afford 5. [α]26D=+190.3 (c=0.1, CHCl3).
後処理
- temperaturewarmed in a reaction flask
- stirringThe reaction mixture was stirred for 10 h at 50° C.
- extractionextracted with CH2Cl2
- dry with materialThe combined organic layers were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo to the dryness
- customThe residue was purified by silica gel (60-230 mesh) column chromatography
- washeluted with 10% ethyl acetate in hexanes
- customto afford 5
出典と根拠
- ORDレコード
- ord-6592f99a6e4c437899ca3e16b3a2ce3a
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09446995B2
反応ノート
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