Hydrochloric Acid → HCID 70592367, compound

HRID 224847Notes

Reaction equation

HRID 224847 reaction equation
C([N:4]1[CH2:8][CH2:7][N:6]=[C:5]1[NH:9][C:10]1[N:14]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[CH:16]=2)[N:13]=[C:12]([CH3:22])[CH:11]=1)(=O)C.Cl>CO>[ClH:21].[Cl:21][C:17]1[CH:16]=[C:15]([N:14]2[C:10]([NH:9][C:5]3[NH:6][CH2:7][CH2:8][N:4]=3)=[CH:11][C:12]([CH3:22])=[N:13]2)[CH:20]=[CH:19][CH:18]=1

Participants

4

Reactant 2

HCID 313Hydrochloric Acid2×HCID 23330488HCID 23330488, compound

Product 1

HCID 70592367HCID 70592367, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

1-Acetyl-2-[1-(3-chlorophenyl)-3-methyl-5-pyrazolyl]amino-2-imidazoline (19.7 g.) was treated with HCl in methanol as described in Example II to give 6.5 g. product as the HCl salt, mp 208°-209°.

Workup

  1. customto give 6.5 g

Sources & evidence

ORD record
ord-7991517776934b93abbf3eff80063cbe
Source dataset
uspto-grants-1980_11
Patent number
US04234594

Reaction notes

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