1,2-Dichloroethane → HCID 66896048, Verbindung

HRID 1257538Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1257538
Cl.[Br:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([C:12]2[CH2:16][C@@H:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=3)[O:14][N:13]=2)[CH:11]=1)[C:6]([OH:8])=O.Cl.[F:24][C:25]1[CH:26]=[CH:27][C:28]([C@H:31]([NH2:33])[CH3:32])=[N:29][CH:30]=1.C(Cl)CCl.C1C=NC2N(O)N=NC=2C=1.C(N(CC)CC)C.C(=O)(O)[O-].[Na+]>CN(C)C=O>[Br:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([C:12]2[CH2:16][C@@H:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=3)[O:14][N:13]=2)[CH:11]=1)[C:6]([NH:33][C@@H:31]([C:28]1[CH:27]=[CH:26][C:25]([F:24])=[CH:30][N:29]=1)[CH3:32])=[O:8]

Komponenten

8

Versuchsvorschrift

To a solution of 3-bromo-5-[(5S)-5-(2-pyridinyl)-4,5-dihydro-3-isoxazolyl]benzoic acid hydrochloride (0.476 g, 1.24 mmol) in N,N-dimethylformamide (6 mL) were added (1R)-1-(5-fluoropyridin-2-yl)ethanamine hydrochloride (0.330 g, 1.55 mmol), EDC (416 mg, 2.17 mmol), HOAT (0.051 g, 0.372 mmol) and triethylamine (0.865 mL, 6.20 mmol). The reaction mixture was stirred at ambient temperature for 18 h. Saturated aqueous sodium bicarbonate was added. The mixture was extracted with dichloromethane (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (50% hexanes/ethyl acetate→0% hexanes/ethyl acetate) gave the title compound (547 mg). MS 468.9 (M+1).

Aufarbeitung

  1. extractionThe mixture was extracted with dichloromethane (3×)
  2. washThe combined organic extracts were washed with brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customPurification by silica gel chromatography (50% hexanes/ethyl acetate→0% hexanes/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-f06d4e334b2845758b451b38a9379bea
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08461185B2

Notizen zur Reaktion

Wird geladen…