HCID 19780332, compound → HCID 10695098, compound

HRID 2081653Notes

Reaction equation

[CH3:1][CH:2]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[NH:13][C:14]([NH:16][C:17]1[N:18](C(=O)C)[N:19]=[C:20]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[N:21]=1)=[O:15])[CH3:3].CC(C1C=CC=C(C(C)C)C=1NC(NC1N(C(=O)C)N=C(CCCCCCCCCCC)N=1)=O)C>>[CH3:12][CH:10]([C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([CH:2]([CH3:1])[CH3:3])[C:5]=1[NH:13][C:14]([NH:16][C:17]1[N:21]=[C:20]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[NH:19][N:18]=1)=[O:15])[CH3:11]

Participants

Reactant 2

HCID 19780332HCID 19780332, compound

HCID 19780333HCID 19780333, compound

Product 1

HCID 10695098HCID 10695098, compound

Procedure

Employing the general method of Example 2 but using N-[2,6-bis(1-methylethyl)phenyl]-N'-(2-acetyl-5-dodecyl-2H-1,2,4-triazol-3-yl)urea instead of N-[2,6-bis(1-methylethyl)phenyl-N'-(2-acetyl-5-undecyl-2H-1,2,4-triazol-3-yl)urea, the title compound was prepared; m.p. 154°-164° C.

Sources & evidence

ORD record: ord-0305326687424869859c1e0620668e66
Source dataset: uspto-grants-1993_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05185358

Reaction notes

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