HCID 23003227, compound → HCID 23003357, compound

HRID 396504Notes

Reaction equation

HRID 396504 reaction equation
[CH3:1][O:2][C:3](=[O:25])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([CH2:14][CH3:15])[CH:12]=2)[NH:7][C:6]=1[C:16]([C:18]1[CH:23]=[C:22]([CH3:24])[CH:21]=[CH:20][N:19]=1)=[O:17].Br[CH2:27]C(C1C=C(CC)C=CN=1)=O>>[CH3:1][O:2][C:3](=[O:25])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([CH2:14][CH3:15])[CH:12]=2)[NH:7][C:6]=1[C:16]([C:18]1[CH:23]=[C:22]([CH2:24][CH3:27])[CH:21]=[CH:20][N:19]=1)=[O:17]

Participants

3

Reactant 2

HCID 23003227HCID 23003227, compoundHCID 230032632-Bromoacetyl-4-ethylpyridine

Product 1

HCID 23003357HCID 23003357, compound

Procedure

The title compound was prepared according to the procedure described in Example 57 from methyl trans-5-ethyl-2-(phenylsulfonylamino)cinnamate (Example 133, step 2) and 2-bromoacetyl-4-ethylpyridine (Preparation is described in Example 57).

Sources & evidence

ORD record
ord-d47142ce604248dbb61ac19942fe0d61
Source dataset
uspto-grants-2003_08
Patent number
US06608070B1

Reaction notes

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