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Carbamate → 3-[5-fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxymethyl]-piperidine-1-carboxylic acid tert-butyl ester

HRID 30410
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 30410
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH2:11][C:10]([CH:15]([O:23][C:24]2[C:32]3[C:27](=[CH:28][CH:29]=[C:30]([F:33])[CH:31]=3)[NH:26][N:25]=2)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[F:22])(C)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].FC1C=C2C(=CC=1)N(C1C=CC=CC=1F)N=C2O.C(OC(N1CCC[C@@H](COS(C)(=O)=O)C1)=O)(C)(C)C.C(=O)([O-])N.Cl>CCOC(C)=O.O1CCOCC1.CO>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH2:11][CH:10]([CH:15]([O:23][C:24]2[C:32]3[C:27](=[CH:28][CH:29]=[C:30]([F:33])[CH:31]=3)[NH:26][N:25]=2)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[F:22])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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Komponenten

9

Edukt 5

HCID 276CarbamateHCID 313Hydrochloric AcidHCID 10108453N-BOC-3(R)-methylsulfonyloxymethyl-piperidineHCID 685314413-[5-fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxymethyl]-3-methyl-piperidine-1-carboxylic acid tert-butyl esterHCID 178518866HCID 178518866, Verbindung

Produkt 1

HCID 68528358
3-[5-fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxymethyl]-piperidine-1-carboxylic acid tert-butyl ester

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 8857Ethyl AcetateLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

3-[5-fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxymethyl]-piperidine-1-carboxylic acid tert-butyl ester was prepared according to the procedure for Intermediate 57 from Intermediate 23 (0.500 g, 2.03 mmol) and (R)-3-methanesulfonyloxymethyl-piperidine-1-carboxylic acid tert-butyl ester (0.655 g, 2.23 mmol). A room temperature stirred solution of carbamate in EtOAc (5.43 ml) was treated with 5.30 ml of a 4.0 M HCl solution in dioxane. The reaction was allowed to stir overnight at room temperature and was concentrated under reduced pressure, triturated with EtOAc and again concentrated under reduced pressure. This process was repeated three times. Recrystallization of the foam was attempted from hexanes/EtOAc and acetone/hexanes without success. The free base was formed by adding Dowex 550A (OH) Anion Exchange Resin to a stirred solution of the salt in MeOH (10 ml). The mixture was stirred for 30 minutes, filtered and the beads washed three times with 20 of methanol. The organic phase was concentrated under reduced pressure to yield 0.3628 g of the free base as a yellow oil. To a stirred solution of the oil in EtOAc (10 ml) was added maleic acid (0.111 g, 1.0 equivalents). A solid precipitated out and the mixture was concentrated under reduced pressure. The solid was triturated with hexanes/Et2O, filtered and washed with Et2O. The white solid was dried in the oven under reduced pressure at 80° C. overnight to yield 0.390 g (69.6%) of the title maleate salt.

Aufarbeitung

  1. concentrationwas concentrated under reduced pressure
  2. customtriturated with EtOAc
  3. concentrationagain concentrated under reduced pressure
  4. customRecrystallization of the foam
  5. customThe free base was formed
  6. stirringThe mixture was stirred for 30 minutes
  7. filtrationfiltered
  8. washthe beads washed three times with 20 of methanol
  9. concentrationThe organic phase was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-2499f75b6d674531bebe1eff687d8a72
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07423054B2

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