HCID 18789285, compound → HCID 18789328, compound

HRID 1106620Notes

Reaction equation

HRID 1106620 reaction equation
C1C2C(=CC=CC=2)CC1C(NC1C=C(C2C=CC(C=C)=CC=2)NN=1)=O.[CH2:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:28][CH:27]1[C:35]([NH:37][C:38]1[CH:42]=[C:41]([C:43]2[CH:48]=[CH:47][C:46]([CH2:49][CH:50]=[CH2:51])=[CH:45][CH:44]=2)[NH:40][N:39]=1)=[O:36]>>[CH2:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:28][CH:27]1[C:35]([NH:37][C:38]1[CH:42]=[C:41]([C:43]2[CH:48]=[CH:47][C:46]([CH2:49][CH2:50][CH3:51])=[CH:45][CH:44]=2)[NH:40][N:39]=1)=[O:36]

Participants

3

Reactant 2

HCID 18789285HCID 18789285, compoundHCID 18789323HCID 18789323, compound

Product 1

HCID 18789328HCID 18789328, compound

Procedure

The title compound was prepared in the same manner as that described in Example 38 except that 3-(2-indanyl)carbonylamino-5-(4-vinylphenyl)pyrazole used in Example 38 was replaced with 3-(2-indanyl)carbonylamino-5-{4-(2-propenyl)phenyl}pyrazole.

Sources & evidence

ORD record
ord-fd74c5d1272944199b376c5529daaeda
Source dataset
uspto-grants-2000_05
Patent number
US06057335

Reaction notes

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