3,5-Dichloro-2-fluoropyridine → Methyl 4-(N-(benzofuran-6-ylmethyl)-N-(3,5-dichloropyridin-2-yl)sulfamoyl)benzoate

HRID 73072

Reaction equation

HRID 73072 reaction equation
[Cl:1][C:2]1[C:3](F)=[N:4][CH:5]=[C:6]([Cl:8])[CH:7]=1.[O:10]1[C:14]2[CH:15]=[C:16]([CH2:19][NH:20][S:21]([C:24]3[CH:33]=[CH:32][C:27]([C:28]([O:30][CH3:31])=[O:29])=[CH:26][CH:25]=3)(=[O:23])=[O:22])[CH:17]=[CH:18][C:13]=2[CH:12]=[CH:11]1>>[O:10]1[C:14]2[CH:15]=[C:16]([CH2:19][N:20]([C:3]3[C:2]([Cl:1])=[CH:7][C:6]([Cl:8])=[CH:5][N:4]=3)[S:21]([C:24]3[CH:33]=[CH:32][C:27]([C:28]([O:30][CH3:31])=[O:29])=[CH:26][CH:25]=3)(=[O:23])=[O:22])[CH:17]=[CH:18][C:13]=2[CH:12]=[CH:11]1

Participants

3

Reactant 2

HCID 27832563,5-Dichloro-2-fluoropyridineHCID 66837871Methyl 4-(N-(benzofuran-6-ylmethyl)sulfamoyl)benzoate

Product 1

HCID 66837856Methyl 4-(N-(benzofuran-6-ylmethyl)-N-(3,5-dichloropyridin-2-yl)sulfamoyl)benzoate

Procedure

The titled compound was prepared according to the procedure described in step-2 of Example 1 from 3,5-dichloro-2-fluoropyridine and methyl 4-(N-(benzofuran-6-ylmethyl)sulfamoyl)benzoate (step-1 of Example 2). LC-MS (method-C) m/z: M+1 obs 490.91; tR=2.75 min.

Sources & evidence

ORD record
ord-5cc5d2aa180948738fffc6df6fd0b0e9
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Linked notes

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