Benzyl chloroformate → HCID 58687102, Verbindung

HRID 2361326Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2361326
[NH2:1][C:2]1[C:3]([F:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[C:5]#[N:6].C(=O)([O-])[O-].[K+].[K+].[C:17](Cl)(=[O:26])[O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C1COCC1>[C:5]([C:4]1[C:3]([F:10])=[C:2]([NH:1][C:17](=[O:26])[O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:9]=[CH:8][CH:7]=1)#[N:6]

Komponenten

5

Versuchsvorschrift

To a light brown solution of 3-amino-2-fluorobenzonitrile (2.7141 g, 19.94 mmol) and potassium carbonate (4.13 g, 29.9 mmol) in THF (166 mL) was syringed benzyl carbonochloridate (4.49 mL, 29.9 mmol) under nitrogen, and the reaction was stirred overnight. The insoluble material was filtered, and the filtrate was concentrated in vacuo. The residue was dissolved in EtOAc (200 mL) and washed with 1 N aqueous HCl (50 mL), water (50 mL) and brine (50 mL), successively. The organic solution was dried over MgSO4 and concentrated in vacuo to give crude product which was stirred in hexanes (75 mL) for 1 hr. The insoluble material was filtered and washed with hexanes to give the desired product (4.4541 g, 16.48 mmol, 83% yield) as a light tan solid.

Aufarbeitung

  1. filtrationThe insoluble material was filtered
  2. concentrationthe filtrate was concentrated in vacuo
  3. dissolutionThe residue was dissolved in EtOAc (200 mL)
  4. washwashed with 1 N aqueous HCl (50 mL), water (50 mL) and brine (50 mL)
  5. dry with materialThe organic solution was dried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customto give crude product which
  8. filtrationThe insoluble material was filtered
  9. washwashed with hexanes

Quellen und Nachweise

ORD-Eintrag
ord-35552c18e5144906aa03d1210beab117
Quelldatensatz
uspto-grants-2014_04
Patentnummer
US08685969B2

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