HCID 59516113, compound → HCID 59516129, compound

HRID 1799410Notes

Reaction equation

HRID 1799410 reaction equation
[C:1]([O:5][C:6]([C:8]1[CH:9]=[N:10][N:11]([CH2:17]C2C=CC(C(OC)=O)=CC=2)[C:12]=1[S:13][CH2:14][CH2:15][CH3:16])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(OC(C1C=NN(C[C:42]2[CH:47]=[CH:46][CH:45]=[C:44]([C:48]([O:50][CH3:51])=[O:49])[CH:43]=2)C=1Cl)=O)(C)(C)C>>[C:1]([O:5][C:6]([C:8]1[CH:9]=[N:10][N:11]([CH2:17][C:42]2[CH:47]=[CH:46][CH:45]=[C:44]([C:48]([O:50][CH3:51])=[O:49])[CH:43]=2)[C:12]=1[S:13][CH2:14][CH2:15][CH3:16])=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 59516113HCID 59516113, compoundHCID 59516125HCID 59516125, compound

Product 1

HCID 59516129HCID 59516129, compound

Procedure

Compound prepared in an analogous manner to Intermediate #46, replacing 5-Chloro-1-(4-methoxycarbonyl-benzyl)-1H-pyrazole-4-carboxylic acid tert-butyl ester with 5-Chloro-1-(3-methoxycarbonyl-benzyl)-1H-pyrazole-4-carboxylic acid tert-butyl ester

Sources & evidence

ORD record
ord-a7a4d464ba8e4cbe93aff0904babb44f
Source dataset
uspto-grants-2013_01
Patent number
US08344016B2

Reaction notes

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