Benzyl Bromide → HCID 11488850, 화합물

HRID 1356202노트

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HRID 1356202 반응식
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:13][C:14]1[CH:19]=[CH:18][C:17]([OH:20])=[C:16]([I:21])[CH:15]=1)[C:10]([OH:12])=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].CCN(C(C)C)C(C)C.[CH2:31](Br)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1.CCCCCC.CCOC(C)=O>CCOC(C)=O>[CH2:31]([O:11][C:10](=[O:12])[C@@H:9]([NH:8][C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7])[CH2:13][C:14]1[CH:19]=[CH:18][C:17]([OH:20])=[C:16]([I:21])[CH:15]=1)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1

참가 물질

6

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온도
90 °C

실험 절차

(2S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-3-iodo-phenyl)-propionic acid (490 mg. 1.2 mmol) of Step A is stirred in EtOAc (3.6 mL) with DIEA (418 μL, 2.4 mmol) at RT under N2. Benzyl bromide (171 μL, 1.44 mmol) is then added and the reaction mixture is then heated to 90° C. overnight. TLC in 3/1 hexane/EtOAc shows complete consumption of starting material (ninhydrin positive) and the appearance of two higher rf spots. The reaction is cooled to RT, diluted with EtOAc and washed with 1N HCl (2×30 mL) and with saturated NaHCO3 (2×30 mL). The organics are dried (MgSO4), filtered and concentrated to provide a mixture of mono- and dibenzylated products. Flash chromatography (3:1 hexane/EtOAc) affords the title compound, (2S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-3-iodo-phenyl)-propionic acid benzyl ester.

후처리

  1. customconsumption of starting material (ninhydrin positive)
  2. temperatureThe reaction is cooled to RT
  3. additiondiluted with EtOAc
  4. washwashed with 1N HCl (2×30 mL) and with saturated NaHCO3 (2×30 mL)
  5. dry with materialThe organics are dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto provide
  9. additiona mixture of mono- and dibenzylated products

출처 및 근거

ORD 기록
ord-a30a2d0ebd524706808224d26c80fdfd
출처 데이터셋
uspto-grants-2003_07
특허 번호
US06586467B2

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