HCID 21924597, compound → HCID 69216084, compound

HRID 900041Notes

Reaction equation

HRID 900041 reaction equation
[CH3:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[C:4]([N:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[NH2:14])[CH:3]=1.C1(N(C2C=CNN=2)N)C=CC=CC=1>>[CH3:1][C:2]1[N:6]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:5]=[C:4]([N:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[NH2:14])[CH:3]=1.[CH3:1][C:2]1[N:6]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:5]=[C:4]([N:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[NH2:14])[CH:3]=1

Participants

3

Procedure

Compound (45) can be prepared by the procedure for Compound (41) except 5-methyl-1-phenyl-3-(1-phenylhydrazino)-pyrazole (2.64 g, 0.01 mole) is replaced with 0.1 mole of 1-phenylhydrazino-pyrazole.

Sources & evidence

ORD record
ord-5d4f58751cab4ab3994a5b2b25f1da65
Source dataset
uspto-grants-2008_04
Patent number
US07358014B2

Reaction notes

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