Dimethylformamide → Oxalyl chloride

HRID 1668567Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1668567
[NH2:1][C:2]1[C:19]([OH:20])=[CH:18][C:5]2[CH2:6][CH2:7][N:8](C(OC(C)(C)C)=[O:12])[CH2:9][CH2:10][C:4]=2[CH:3]=1.[F:21][C:22]([F:28])([F:27])[CH2:23][C:24]([Cl:26])=[O:25].CN([CH:32]=[O:33])C.[Cl:34]C1C=CC=CC=1>>[F:21][C:22]([F:28])([F:27])[CH2:23][C:24]1[O:20][C:19]2[C:2]([N:1]=1)=[CH:3][C:4]1[CH2:10][CH2:9][NH:8][CH2:7][CH2:6][C:5]=1[CH:18]=2.[F:21][C:22]([F:28])([F:27])[CH2:23][C:24]([OH:12])=[O:25].[C:32]([Cl:34])(=[O:33])[C:24]([Cl:26])=[O:25]

Komponenten

7

Edukt 4

HCID 6228DimethylformamideHCID 7964ChlorobenzeneHCID 27833433,3,3-Trifluoropropionyl chlorideHCID 591504721,1-Dimethylethyl 7-amino-8-hydroxy-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate

Produkt 3

HCID 65578Oxalyl chlorideHCID 27779723,3,3-Trifluoropropionic acidHCID 591504962-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydro-5H-[1,3]oxazolo[4,5-h][3]benzazepine

Versuchsvorschrift

The title compound was prepared as described in General Procedure 2 from 1,1-dimethylethyl 7-amino-8-hydroxy-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate and 3,3,3-trifluoropropanoyl chloride. The latter reactant had been obtained in chlorobenzene solution from the reaction of 3,3,3-trifluoropropanoic acid with oxalyl chloride (1 eq.) in the presence of a catalytic quantity of DMF.

Quellen und Nachweise

ORD-Eintrag
ord-4394e2537b9c401f8d35b76812a2d200
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US07989444B2

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