Sodium borohydride → HCID 22098743, compound

HRID 2260863Notes

Reaction equation

HRID 2260863 reaction equation
Cl.[C:2]([C:5]1[CH:10]=[CH:9][C:8]([C:11]([CH2:13][N:14]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])[C:15]2=[O:26])=[O:12])=[CH:7][CH:6]=1)(=[NH:4])[NH2:3].[BH4-].[Na+]>CO>[C:2]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]([OH:12])[CH2:13][N:14]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])[C:15]2=[O:26])=[CH:7][CH:6]=1)(=[NH:3])[NH2:4]

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 22098390HCID 22098390, compound

Product 1

HCID 22098743HCID 22098743, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Prepared by reduction of 1-[(4-amidino-phenyl)-carbonyl-methyl]-3-(3-methoxycarbonyl-propyl)-imidazolidin-2-one hydrochloride with sodium borohydride in methanol at 0°-5° C.

Sources & evidence

ORD record
ord-781156e090e14853b170e981519b693c
Source dataset
uspto-grants-1995_12
Patent number
US05478942

Reaction notes

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