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Diisopropylethylamine → N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-6-methoxy-N-methyl-1H-indazole-3-carboxamide

HRID 2383395
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2383395
[CH3:1][O:2][C:3]1[CH:14]=C[C:6]2[C:7]([C:10](O)=[O:11])=[N:8]S[C:5]=2[CH:4]=1.[CH:15](N(C(C)C)CC)(C)C.Cl.Cl.[NH2:26][C@@H:27]1[CH:32]2[CH2:33][CH2:34][N:29]([CH2:30][CH2:31]2)[CH2:28]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.O1CCCC1.C[N:65]([CH3:68])C=O>>[N:29]12[CH2:34][CH2:33][CH:32]([CH2:31][CH2:30]1)[C@H:27]([N:26]([CH3:15])[C:10]([C:7]1[C:6]3[C:68](=[CH:14][C:3]([O:2][CH3:1])=[CH:4][CH:5]=3)[NH:65][N:8]=1)=[O:11])[CH2:28]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 12494972(R)-(+)-3-Aminoquinuclidine DihydrochlorideHCID 21974620tetrahydrofuran N,N-dimethylformamideHCID 666368056-Methoxybenzo[d]isothiazole-3-carboxylic acid

Produkt 1

HCID 16660032N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-6-methoxy-N-methyl-1H-indazole-3-carboxamideAusbeute 75 %

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 6-methoxybenzisothiazole-3-carboxylic acid (61 mg, 0.30 mmol) in a 5/1 mixture of tetrahydrofuran/N,N-dimethylformamide (12 mL) was added diisopropylethylamine (0.2 mL, 1.1 mmol) and (115 mg, 0.6 mmol) 3-(R)-aminoquinuclidine dihydrochloride. The mixture was cooled to 0° C., and HATU (115 mg, 0.3 mmol) was added in one portion. The reaction mixture was allowed to warm to rt and was maintained overnight. The mixture was partitioned between saturated aqueous potassium carbonate solution and a 95/5 mixture of dichloromethane/methanol. The aqueous layer was extracted with 95/5 dichloromethane/methanol (2×), and the combined organic layers were washed with brine and dried over sodium sulfate. The crude product was purified by chromatography (90/10/1 dichloromethane/methanol/ammonium hydroxide) or by preparative HPLC, thus providing the amide in 75% yield as a colorless solid.

Aufarbeitung

  1. temperatureto warm to rt
  2. temperaturewas maintained overnight
  3. customThe mixture was partitioned between saturated aqueous potassium carbonate solution
  4. additiona 95/5 mixture of dichloromethane/methanol
  5. extractionThe aqueous layer was extracted with 95/5 dichloromethane/methanol (2×)
  6. washthe combined organic layers were washed with brine
  7. dry with materialdried over sodium sulfate
  8. customThe crude product was purified by chromatography (90/10/1 dichloromethane/methanol/ammonium hydroxide) or by preparative HPLC

Quellen und Nachweise

ORD-Eintrag
ord-2485b65d3f8047bb9a7fc484fabe0df0
Quelldatensatz
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08263619B2

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