Hydrochloric Acid → [3-((3R,6R)-5-Amino-3,6-dimethyl-6-trifluoromethyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-4-fluoro-phenyl]-(7-chloro-pyrido[3,2-d]pyrimidin-4-yl)-amine di-hydrochloride

HRID 925462Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 925462
C(OC(=O)[NH:7][C:8]1[C@:9]([CH3:27])([C:23]([F:26])([F:25])[F:24])[O:10][CH2:11][C@:12]([C:15]2[CH:20]=[C:19]([NH2:21])[CH:18]=[CH:17][C:16]=2[F:22])([CH3:14])[N:13]=1)(C)(C)C.[Cl:29][C:30]1[C:31]2[N:39]=[CH:38][C:37]([Cl:40])=[CH:36][C:32]=2[N:33]=[CH:34][N:35]=1.[ClH:41].C([O-])(O)=O.[Na+]>CC(O)(C)C.O1CCOCC1>[ClH:29].[ClH:41].[NH2:7][C:8]1[C@:9]([CH3:27])([C:23]([F:24])([F:25])[F:26])[O:10][CH2:11][C@:12]([C:15]2[CH:20]=[C:19]([NH:21][C:30]3[C:31]4[N:39]=[CH:38][C:37]([Cl:40])=[CH:36][C:32]=4[N:33]=[CH:34][N:35]=3)[CH:18]=[CH:17][C:16]=2[F:22])([CH3:14])[N:13]=1

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 66666212[(2R,5R)-5-(5-Amino-2-fluoro-phenyl)-2,5-dimethyl-2-trifluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl esterHCID 714284454,7-Dichloropyrido[3,2-d]pyrimidine

Produkt 1

HCID 71550948[3-((3R,6R)-5-Amino-3,6-dimethyl-6-trifluoromethyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-4-fluoro-phenyl]-(7-chloro-pyrido[3,2-d]pyrimidin-4-yl)-amine di-hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6386tert-ButanolLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a solution of [(2R,5R)-5-(5-amino-2-fluoro-phenyl)-2,5-dimethyl-2-trifluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester (CAS registry 1262859-70-0) (138 mg, 0.34 mmol) and 4,7-dichloro-pyrido[3,2-d]pyrimidine (CAS registry 917757-12-1) (75 mg, 0.374 mmol) in tBuOH (2 ml) was added 0.1 ml 4N HCl in dioxane and the reaction mixture was heated in a microwave oven for 1 h at 100° C. The reaction mixture was basified with saturated NaHCO3 solution and the product was extracted with EtOAc. Combined extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was dissolved in THF, acidified with 1N HCl in Et2O, and concentrated. The remaining yellow solid was two times triturated with Et2O and subsequently dried to afford the title compound as light yellow amorphous solid.

Aufarbeitung

  1. extractionthe product was extracted with EtOAc
  2. washCombined extracts were washed with brine
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. dissolutionThe crude product was dissolved in THF
  7. concentrationconcentrated
  8. customtriturated with Et2O
  9. customsubsequently dried

Quellen und Nachweise

ORD-Eintrag
ord-32699ed361a3467684f8903a50c01193
Quelldatensatz
uspto-grants-2016_03
Patentnummer
US09284284B2

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