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tert-butyl N-(4-aminobutyl)carbamate → HCID 68186050, Verbindung

HRID 628969
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 628969
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:14]3[CH:15]=[C:16]([O:19][CH3:20])[CH:17]=[CH:18][C:13]=3[N:12]3[C:21]([CH3:24])=[N:22][N:23]=[C:11]3[C@H:10]([CH2:25][C:26]([OH:28])=O)[N:9]=2)=[CH:4][CH:3]=1.CN(C(O[N:37]1N=N[C:39]2[CH:40]=[CH:41][CH:42]=[N:43][C:38]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.NCCCCN[C:68](=[O:74])[O:69][C:70]([CH3:73])([CH3:72])[CH3:71]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:14]3[CH:15]=[C:16]([O:19][CH3:20])[CH:17]=[CH:18][C:13]=3[N:12]3[C:21]([CH3:24])=[N:22][N:23]=[C:11]3[C@H:10]([CH2:25][C:26]([NH:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][NH:43][C:68](=[O:74])[O:69][C:70]([CH3:73])([CH3:72])[CH3:71])=[O:28])[N:9]=2)=[CH:6][CH:7]=1
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Komponenten

5

Edukt 4

HCID 4351tert-butyl N-(4-aminobutyl)carbamateHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 67173666I-BET762 carboxylic acid

Produkt 1

HCID 68186050HCID 68186050, Verbindung

Versuchsvorschrift

A mixture of [(4S)-6-(4-chlorophenyl)-1-methyl-8-(methyloxy)-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]acetic acid (for a preparation see Reference compound G) (1.0 g, 2.5 mmol), HATU (1.9 g, 5 mmol) and DIPEA (0.88 ml, 5 mmol) was stirred for 80 minutes at room temperature, to this was added 1,1-dimethylethyl (4-aminobutyl)carbamate (1.05 ml, 5.0 mmol, available from Aldrich). The reaction mixture was stirred at room temperature for 2 h before it was concentrated. The residue was taken up in dichloromethane and washed with 1N HCl. The aqueous layer was extracted with dichloromethane twice. Organic layer was washed with 1N sodium hydroxide, followed by a saturated solution of sodium chloride, dried over sodium sulphate and concentrated. The residue was purified by flash-chromatography on silica using dichloromethane/methanol 95/5 to give the title compound as a yellow solid (1.2 g). LC/MS (Method D): rt=3.04 min.

Aufarbeitung

  1. stirringThe reaction mixture was stirred at room temperature for 2 h before it
  2. concentrationwas concentrated
  3. washwashed with 1N HCl
  4. extractionThe aqueous layer was extracted with dichloromethane twice
  5. washOrganic layer was washed with 1N sodium hydroxide
  6. dry with materialdried over sodium sulphate
  7. concentrationconcentrated
  8. customThe residue was purified by flash-chromatography on silica

Quellen und Nachweise

ORD-Eintrag
ord-ef4323c4ed144d6db325e3e88a0897ed
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09315487B2

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