2-Chloromethyl-4-(2-furylmethylthio)-3-methylpyridine hydrochloride → HCID 178431892, compound

HRID 1081677Notes

Reaction equation

HRID 1081677 reaction equation
[ClH:1].[Cl:2][CH2:3][C:4]1[C:9]([CH3:10])=[C:8]([S:11][CH2:12][C:13]2[O:14][CH:15]=[CH:16][CH:17]=2)[CH:7]=[CH:6][N:5]=1.[SH:18][C:19]1[NH:23][C:22]2[CH:24]=[CH:25][C:26]([C:28]([F:31])([F:30])[F:29])=[CH:27][C:21]=2[N:20]=1>C(O)(C)C>[ClH:2].[ClH:1].[O:14]1[CH:15]=[CH:16][CH:17]=[C:13]1[CH2:12][S:11][C:8]1[CH:7]=[CH:6][N:5]=[C:4]([CH2:3][S:18][C:19]2[NH:23][C:22]3[CH:24]=[CH:25][C:26]([C:28]([F:31])([F:30])[F:29])=[CH:27][C:21]=3[N:20]=2)[C:9]=1[CH3:10]

Participants

4

Reactant 2

HCID 224607712-Chloromethyl-4-(2-furylmethylthio)-3-methylpyridine hydrochlorideHCID 178506092HCID 178506092, compound

Product 1

HCID 178431892HCID 178431892, compound

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

Following the procedure described in Example 12, the reaction of 2-chloromethyl-4-(2-furylmethylthio)-3-methylpyridine hydrochloride with 2-mercapto-5-trifluoromethyl-1H-benzimidazole in isopropanol gives the title compound as a colorless solid; m.p. 173° C (decomp.).

Sources & evidence

ORD record
ord-1085681f87bd42ddb4e5e17f7bc6f304
Source dataset
uspto-grants-1996_12
Patent number
US05587389

Reaction notes

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