Ethanol → HCID 69817666、化合物

HRID 2417410ノート

反応式

HRID 2417410 の反応式
[CH2:1]([N:8](C(O)CCC1C=CC([N+]([O-])=O)=CC=1)[CH2:9][C@H:10]([OH:19])[CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.[Cl-].[NH4+:35].[CH2:36]([OH:38])[CH3:37]>[Fe]>[NH2:35][C:5]1[CH:6]=[CH:7][C:2]([CH2:1][C@H:37]([N:8]([CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:9][C@H:10]([OH:19])[CH2:11][O:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:36][OH:38])=[CH:3][CH:4]=1

参加物

6

実験手順

To a suspension of (2S)-2-[(N-benzyl-N-((2S)-2-hydroxy-3-phenoxypropyl]amino]-3-(4-nitrophenyl)-1-propanol (1.12 g) in ethanol (11 ml)—water (2.2 ml) were added powdered iron (573 mg) and ammonium chloride (55 mg). The mixture was gently heated to reflux for 1 hour and allowed to cool to room temperature. After the insoluble material was filtered off, the filtrate was concentrated and partitioned between chloroform and water. The organic layer was separated, washed successively with water and brine, dried over magnesium sulfate, and filtered. The filtrate was concentrated and the residue was purified by column chromatography (silica gel, hexane/ethyl acetate) to give (2S)-3-(4-aminophenyl)-2-[N-benzyl-N-[(2S)-2-hydroxy-3-phenoxypropyl]amino]-1-propanol (990 mg) as a pale yellow oil.

後処理

  1. temperatureThe mixture was gently heated
  2. temperatureto reflux for 1 hour
  3. filtrationAfter the insoluble material was filtered off
  4. concentrationthe filtrate was concentrated
  5. custompartitioned between chloroform and water
  6. customThe organic layer was separated
  7. washwashed successively with water and brine
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated
  11. customthe residue was purified by column chromatography (silica gel, hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-41d7adc3ff60447296ec2d93e77947da
出典データセット
uspto-grants-2004_11
特許番号
US06826033B2

反応ノート

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