2,6-Difluorobenzaldehyde → Methyl(S)-3-[4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]phenyl]-2-(2,6-difluorobenzylamino)propionate

HRID 585531Notes

Reaction equation

HRID 585531 reaction equation
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][C:10](C)=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:14][CH2:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][C@H:24]([NH:30][CH2:31]C2C=CC(F)=CC=2)[C:25]([O:27][CH2:28]C)=[O:26])=[CH:19][CH:18]=1.[F:39][C:40]1[CH:47]=[CH:46][CH:45]=[C:44]([F:48])[C:41]=1C=O>>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:14][CH2:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][C@H:24]([NH:30][CH2:31][C:41]2[C:40]([F:39])=[CH:47][CH:46]=[CH:45][C:44]=2[F:48])[C:25]([O:27][CH3:28])=[O:26])=[CH:19][CH:18]=1

Participants

3

Procedure

In the same manner as in Example 7, 570.3 mg of the title compound was obtained as colorless powder from 600.8 mg of Referential Compound 3 and 220 μL of 2,6-difluorobenzaldehyde.

Sources & evidence

ORD record
ord-0a5a13dd6eb64d98a9b60c256370a973
Source dataset
uspto-grants-2005_08
Patent number
US06933309B2

Reaction notes

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