Hydrochloric Acid → HCID 57980031, 화합물

HRID 1867811노트

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HRID 1867811 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][C:13]([C:16]([N:18]3[CH2:22][CH2:21][CH2:20][C@H:19]3[CH2:23][N:24]3[CH2:28][CH2:27][CH2:26][CH2:25]3)=[O:17])=[CH:12][CH:11]=2)=[CH:6][CH:5]=1)([O-])=O.O.O.Cl[Sn]Cl.Cl>CCO>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]([C:16]([N:18]3[CH2:22][CH2:21][CH2:20][C@H:19]3[CH2:23][N:24]3[CH2:25][CH2:26][CH2:27][CH2:28]3)=[O:17])=[CH:14][CH:15]=2)=[CH:6][CH:5]=1

참가 물질

5

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온도
60 °C

실험 절차

Procedure OO: 160 mg of (4′-Nitro-biphenyl-4-yl)-(2-(S)-pyrrolidin-1-ylmethyl-pyrrolidin-1-yl)-methanone (0.43 mmol) is put into the solution of 485 mg of SnCl2.2H2O (2.15 mmol) in 1.0 ml of EtOH. 1.0 ml of conc. HCl is added to the mixture and heated at 60° C. for 30 min. EtOH is removed in vacuo and the solution is made it to pH=12.0 by aqueous NaOH. This mixture is extracted with dichloromethane, dried over Na2SO4 and evaporated. The crude product is applied to SCX column and washed by MeOH and the desired product is eluted with 2M NH3 in MeOH. The elution is concentrated and applied to silica-gel column chromatography (CH2Cl2:2M NH3 in MeOH=20:1) to give the title compound. 77 mg (51%) Observed mass; 350 (M+1)

후처리

  1. customEtOH is removed in vacuo
  2. extractionThis mixture is extracted with dichloromethane
  3. dry with materialdried over Na2SO4
  4. customevaporated
  5. washwashed by MeOH
  6. washthe desired product is eluted with 2M NH3 in MeOH
  7. washThe elution
  8. concentrationis concentrated

출처 및 근거

ORD 기록
ord-dde131494d77491ebe1b5fcc25d9320b
출처 데이터셋
uspto-grants-2009_12
특허 번호
US07632857B2

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