Hydrochloric Acid → HCID 57461383, compound

HRID 1459073Notes

Reaction equation

[C:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:14][CH2:13][N:12]([C:15]3[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][C:23]([OH:25])=[O:24])=[CH:17][CH:16]=3)[C:11]2=[O:26])=[CH:6][CH:5]=1)(=[NH:3])[NH2:2].[ClH:27].[Cl-].[Na+].[CH3:30]O>>[ClH:27].[C:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:14][CH2:13][N:12]([C:15]3[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][C:23]([O:25][CH3:30])=[O:24])=[CH:17][CH:16]=3)[C:11]2=[O:26])=[CH:6][CH:5]=1)(=[NH:2])[NH2:3]

Participants

Reactant 4

HCID 313Hydrochloric Acid

HCID 887Methanol

HCID 5234Sodium Chloride

HCID 9798587HCID 9798587, compound

Product 1

HCID 57461383HCID 57461383, compound

Procedure

Melting point: from 260° C. (decomp.) The product was also obtained by reacting 1-(4-amidino-phenyl)-3-[4-(2-carboxy-ethyl)-phenyl]-imidazolidin-2-one with methanolic hydrochloric acid. Rf value: 0.49 (Reversed Phase Plate RP8; 10% sodium chloride solution/methanol=4:6)

Sources & evidence

ORD record: ord-dac9c4eded7c45b7ab14f17760798267
Source dataset: uspto-grants-1998_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05852192

Reaction notes

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