Hydrochloric Acid → 2-[(4-Nitrophenyl)thio]-1-phenyl-1H-imidazole hydrochloride

HRID 1074197Notes

Reaction equation

HRID 1074197 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10][C:11]2[N:12]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH:13]=[CH:14][N:15]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[ClH:22]>>[ClH:22].[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10][C:11]2[N:12]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH:13]=[CH:14][N:15]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 150774972-[(4-Nitrophenyl)thio]-1-phenyl-1H-imidazole

Product 1

HCID 221559862-[(4-Nitrophenyl)thio]-1-phenyl-1H-imidazole hydrochloride

Procedure

The product from Example 24 was converted to the hydrochloride salt by treatment with ethanolic hydrogen chloride. After recrystallization from methanol/isopropanol/ether the product was obtained off-white prisms, mp 215°-218° C.

Workup

  1. customAfter recrystallization from methanol/isopropanol/ether the product
  2. customwas obtained off-white prisms, mp 215°-218° C.

Sources & evidence

ORD record
ord-7d9e1ea2855c401a9e1f18b748e65495
Source dataset
uspto-grants-1990_11
Patent number
US04973599

Reaction notes

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