Ammonia → HCID 86651606, Verbindung

HRID 1867330Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1867330
[C:1](Cl)(Cl)=[O:2].[OH:5][C:6]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[NH:19][CH2:20][CH2:21][C:22]([NH:25][C:26](=[O:32])[O:27][C:28]([CH3:31])([CH3:30])[CH3:29])([CH3:24])[CH3:23])([CH2:10][CH2:11][CH3:12])[CH2:7][CH2:8][CH3:9].C(N(CC)CC)C.N>C1COCC1.CCOC(C)=O>[C:28]([O:27][C:26](=[O:32])[NH:25][C:22]([CH3:23])([CH3:24])[CH2:21][CH2:20][N:19]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[C:6]([CH2:7][CH2:8][CH3:9])([CH2:10][CH2:11][CH3:12])[O:5][C:1]1=[O:2])([CH3:30])([CH3:29])[CH3:31]

Komponenten

7

Versuchsvorschrift

8.85 mL (16.81 mmol) of phosgene solution (20 wt. % in toluene) is slowly added dropwise at 0° C. to a solution of 6.00 g (15.28 mmol) of tert-butyl {3-[2-(1-hydroxy-1-propylbutyl)phenylamino]-1,1-dimethylpropyl}carbamate and 5.32 mL (38.21 mmol) of triethylamine in absolute THF (80 mL). The mixture is stirred for 2 hours at RT, diluted with EtOAc, combined with ice, and made basic with saturated aqueous ammonia solution. The aqueous phase is exhaustively extracted with EtOAc and the combined organic phases are washed with saturated aqueous NaCl, dried with sodium sulfate, and evaporated down in vacuo. After column chromatography (silica gel, cyclohexane/EtOAc 6:1) the product is obtained as a yellow oil. Yield: 4.57 g (71%).

Aufarbeitung

  1. extractionThe aqueous phase is exhaustively extracted with EtOAc
  2. washthe combined organic phases are washed with saturated aqueous NaCl
  3. dry with materialdried with sodium sulfate
  4. customevaporated down in vacuo
  5. customAfter column chromatography (silica gel, cyclohexane/EtOAc 6:1) the product is obtained as a yellow oil

Quellen und Nachweise

ORD-Eintrag
ord-bb40f34fc136417cb756bfccf000e995
Quelldatensatz
uspto-grants-2009_12
Patentnummer
US07632834B2

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