Naphthalene → 1-(3-(t-butoxy-carbonylamino)-2-(N-methyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)propyl)cyclohexanol

HRID 2355440노트

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HRID 2355440 반응식
[OH:1][C:2]1([CH2:8][CH:9]([NH:19][CH3:20])[CH2:10][NH:11][C:12](=[O:18])[O:13][C:14]([CH3:17])([CH3:16])[CH3:15])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.C1C2C(=CC=CC=2)C=CC=1.C([O-])([O-])=O.[K+].[K+].[C:37]([O:46]N1C(=O)CCC1=O)([O:39][CH2:40][CH2:41][Si:42]([CH3:45])([CH3:44])[CH3:43])=O>C1COCC1.O>[C:14]([O:13][C:12]([NH:11][CH2:10][CH:9]([N:19]([CH3:20])[C:37]([O:39][CH2:40][CH2:41][Si:42]([CH3:43])([CH3:44])[CH3:45])=[O:46])[CH2:8][C:2]1([OH:1])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1)=[O:18])([CH3:16])([CH3:17])[CH3:15]

참가 물질

6

실험 절차

To a solution of above mixture of tert-butyl 3-(1-hydroxycyclohexyl)-2-(methylamino)-propylcarbamate and naphthalene in 3:1 THF/H2O V/V (4 mL) was added K2CO3 (100 mg, 0.72 mmol), followed by Teoc-OSu (70 mg, 0.27 mmol). The resulting solution was stirred at rt for 30 min and the organic solvent was removed under reduced pressure. The residue was extracted with EtOAc (2×). The combined organic phases were washed with brine, dried, filtered, and concentrated under vacuum. The residue was chromatographed on silica gel to give 1-(3-(t-butoxycarbonylamino)-2-(N-methyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)propyl)cyclohexanol (100 mg, 86% for three steps). MS m/z 453 (M+Na+).

후처리

  1. customthe organic solvent was removed under reduced pressure
  2. extractionThe residue was extracted with EtOAc (2×)
  3. washThe combined organic phases were washed with brine
  4. customdried
  5. filtrationfiltered
  6. concentrationconcentrated under vacuum
  7. customThe residue was chromatographed on silica gel

출처 및 근거

ORD 기록
ord-79826e4760e5418b9c0352e2844553e1
출처 데이터셋
uspto-grants-2010_07
특허 번호
US07754737B2

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