HCID 15453701, compound → HCID 23003466, compound

HRID 396509Notes

Reaction equation

HRID 396509 reaction equation
C1(S([NH:10][C:11]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][C:12]=2/[CH:13]=[CH:14]/[C:15]([O:17][CH3:18])=[O:16])(=O)=O)C=CC=CC=1.Br[CH2:28][C:29]([C:31]1[CH:36]=[C:35]([CH2:37][CH3:38])[CH:34]=[CH:33][N:32]=1)=[O:30]>>[CH3:18][O:17][C:15](=[O:16])[CH2:14][C:13]1[C:12]2[C:11](=[CH:22][CH:21]=[C:20]([C:23]([F:24])([F:25])[F:26])[CH:19]=2)[NH:10][C:28]=1[C:29]([C:31]1[CH:36]=[C:35]([CH2:37][CH3:38])[CH:34]=[CH:33][N:32]=1)=[O:30]

Participants

3

Reactant 2

HCID 15453701HCID 15453701, compoundHCID 230032632-Bromoacetyl-4-ethylpyridine

Product 1

HCID 23003466HCID 23003466, compound

Procedure

The title compound was prepared according to the procedure described in Example 57 from methyl trans-2-phenylsulfonylamino-5-(trifluoromethyl)cinnamate (step 2 of Example 151) and 2-bromoacetyl-4-ethylpyridine (Preparation is described in Example 57).

Sources & evidence

ORD record
ord-d2c216a516894e1bbabdc96d0891ab71
Source dataset
uspto-grants-2003_08
Patent number
US06608070B1

Reaction notes

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