Isobutylamine → HCID 18316023, compound

HRID 276680Notes

Reaction equation

HRID 276680 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[N:11]=[C:12]=[S:13].[CH2:14]([NH2:18])[CH:15]([CH3:17])[CH3:16].Cl[CH:20]([CH:24]([CH3:26])[CH3:25])[C:21](O)=[O:22]>>[CH3:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[N:11]=[C:12]1[N:18]([CH2:14][CH:15]([CH3:17])[CH3:16])[C:21](=[O:22])[CH:20]([CH:24]([CH3:26])[CH3:25])[S:13]1

Participants

4

Reactant 3

HCID 6558IsobutylamineHCID 1456212-Methyl-4-nitrophenyl isothiocyanateHCID 3134932-chloro-3-methylbutanoic acid

Product 1

HCID 18316023HCID 18316023, compound

Procedure

2-Methyl-4-nitrophenyl isothiocyanate was reacted with isobutylamine followed by 2-chloro-3-methylbutanoic acid according to Method C8a to afford 2-(2-methyl-4-nitrophenylimino)-3-isobutyl-5-isopropyl-1,3-thiazolidin-4-one.

Sources & evidence

ORD record
ord-616ce96f549f40b38a32004b16dfcd8c
Source dataset
uspto-grants-2002_03
Patent number
US06353006B1

Reaction notes

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