Hexylamine → HCID 178444848, compound

HRID 1636349Notes

Reaction equation

[CH2:1]([C:3]1[CH:26]=[CH:25][CH:24]=[CH:23][C:4]=1[NH:5][CH:6]=[C:7]1[C:11](=[O:12])[N:10]([C:13]2[CH:21]=[CH:20][C:16]([C:17](O)=[O:18])=[CH:15][CH:14]=2)[N:9]=[C:8]1[CH3:22])[CH3:2].[CH2:27]([NH2:33])[CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]>>[CH2:1]([C:3]1[CH:26]=[CH:25][CH:24]=[CH:23][C:4]=1[NH:5][CH:6]=[C:7]1[C:11](=[O:12])[N:10]([C:13]2[CH:14]=[CH:15][C:16]([C:17]([NH:33][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[O:18])=[CH:20][CH:21]=2)[N:9]=[C:8]1[CH3:22])[CH3:2]

Participants

Reactant 2

HCID 8102Hexylamine

HCID 178436089HCID 178436089, compound

Product 1

HCID 178444848HCID 178444848, compound

Procedure

From the reaction of 4-(4-(2-ethylanilinomethylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)-benzoic acid and hexylamine, 4-(4-(2-ethylanilinomethylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)-N-hexylbenzamide is obtained, Mp 62.1° C.

Sources & evidence

ORD record: ord-8af4728f40ff418091f517e90d76158e
Source dataset: uspto-grants-2000_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06034099

Reaction notes

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