2-Bromo-6-(methoxymethyl)pyridine → HCID 59526156, compound

HRID 385842Notes

Reaction equation

HRID 385842 reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][O:9][CH3:10])[N:3]=1.[NH2:11][C:12]1[S:13][C:14]([C:20]2[CH:25]=[C:24]([Cl:26])[CH:23]=[CH:22][C:21]=2[Cl:27])=[CH:15][C:16]=1[C:17]([NH2:19])=[O:18]>>[Cl:27][C:21]1[CH:22]=[CH:23][C:24]([Cl:26])=[CH:25][C:20]=1[C:14]1[S:13][C:12]([NH:11][C:2]2[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][O:9][CH3:10])[N:3]=2)=[C:16]([C:17]([NH2:19])=[O:18])[CH:15]=1

Participants

3

Reactant 2

HCID 109435402-Bromo-6-(methoxymethyl)pyridineHCID 595257103-Thiophenecarboxamide, 2-amino-5-(2,5-dichlorophenyl)-

Product 1

HCID 59526156HCID 59526156, compound

Procedure

The title compound was prepared as described in Example 1 using 2-bromo-6-(methoxymethyl)pyridine (105 mg, 0.520 mmol) (for preparation, see Journal of Organic Chemistry 1993, 58, 4389-97) and 2-amino-5-(2,5-dichlorophenyl)thiophene-3-carboxamide (152 mg, 0.530 mmol) as starting materials.

Sources & evidence

ORD record
ord-6c41c6c3f76c413ba40dfc65b50cd18a
Source dataset
uspto-grants-2013_02
Patent number
US08367706B2

Reaction notes

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