Dichloromethane → (4-fluorotetrahydro-2H-pyran-4-yl)methanamine
Reaktionsgleichung
[F:1][C:2]1([CH2:8][N:9]2C(=O)C3C(=CC=CC=3)C2=O)[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.NN.C(Cl)Cl>C(O)C>[F:1][C:2]1([CH2:8][NH2:9])[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of EXAMPLE 337B (1.4 g) and hydrazine (1.548 mL) in ethanol (40 mL) was heated at 70° C. overnight, cooled to room temperature, slurried with CH2Cl2 (200 mL) and the solid removed by filtration. The filtrate was concentrated and chromatographed on silica gel with 100:5:1 ethyl acetate/methanol/NH4OH as eluent to give the product.
Aufarbeitung
- customthe solid removed by filtration
- concentrationThe filtrate was concentrated
- customchromatographed on silica gel with 100:5:1 ethyl acetate/methanol/NH4OH as eluent
- customto give the product
Quellen und Nachweise
- ORD-Eintrag
- ord-1184d2459e3a41a5808bc561387d0b80
- Quelldatensatz
- uspto-grants-2015_05
- Patentnummer
- US09029404B2
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