HCID 23442354, compound → HCID 23442342, compound

HRID 2119636Notes

Reaction equation

HRID 2119636 reaction equation
[CH3:1][O:2][C:3]1[CH:27]=[CH:26][CH:25]=[CH:24][C:4]=1[CH2:5][C:6]1[CH:7]=[CH:8][C:9]([N+:21]([O-])=O)=[C:10]([C:12]([C:14]2[N:18]([CH3:19])[N:17]=[CH:16][C:15]=2I)=[O:13])[CH:11]=1.ClC1C=CC(CC2C=CC([N+]([O-])=O)=C(C(C3N(C)N=CC=3I)=O)C=2)=CC=1>>[CH3:1][O:2][C:3]1[CH:27]=[CH:26][CH:25]=[CH:24][C:4]=1[CH2:5][C:6]1[CH:7]=[CH:8][C:9]2[NH:21][C:15]3[CH:16]=[N:17][N:18]([CH3:19])[C:14]=3[C:12](=[O:13])[C:10]=2[CH:11]=1

Participants

3

Reactant 2

HCID 23442354HCID 23442354, compoundHCID 23442417HCID 23442417, compound

Product 1

HCID 23442342HCID 23442342, compound

Procedure

The title compound was prepared according to the procedure of step 5 in EXAMPLE 13 using [5-(2-methoxybenzyl)-2-nitrophenyl](4-iodo-1-methyl-1H-pyrazol-5-yl)methanone (EXAMPLE 21, step 3), instead of [5-(4-chlorobenzyl)-2-nitrophenyl](4-iodo-1-methyl-1H-pyrazol-5-yl)methanone.

Sources & evidence

ORD record
ord-fdfb41742b334d8b91223e637ffc86ca
Source dataset
uspto-grants-2004_02
Patent number
US06686373B2

Reaction notes

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