4-methoxy-1H-pyrazole → HCID 178494727, compound

HRID 1488185Notes

Reaction equation

HRID 1488185 reaction equation
COC1C=NNC=1[C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][C:17]=1[CH3:18])[C:11]([O:13][CH3:14])=[O:12].[Cl:19][C:20]1[C:21]([CH2:25][O:26][CH3:27])=[N:22][NH:23][CH:24]=1.[CH3:28]OC1C=NNC=1>>[Cl:19][C:20]1[C:21]([CH2:25][O:26][CH3:27])=[N:22][NH:23][C:24]=1[C:16]1[C:17]([CH3:18])=[CH:8][C:9]([CH3:28])=[C:10]([CH:15]=1)[C:11]([O:13][CH3:14])=[O:12]

Participants

4

Reactant 3

HCID 53247764-methoxy-1H-pyrazoleHCID 90030202Methyl 3-(4-methoxy-1H-pyrazol-5-yl)-4-methylbenzoateHCID 178494718HCID 178494718, compound2×

Product 1

HCID 178494727HCID 178494727, compound

Procedure

The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 244.6, except 4-chloro-3-(methoxymethyl)-1H-pyrazole (compound 281.2) was used instead of 4-methoxy-1H-pyrazole (compound 244.4).

Sources & evidence

ORD record
ord-5de93e95023f4c8398de15eddc55e907
Source dataset
uspto-grants-2016_08
Patent number
US09428502B2

Reaction notes

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