HCID 19623797, compound → HCID 58446922, compound

HRID 1802311Notes

Reaction equation

HRID 1802311 reaction equation
[CH3:1][N:2]([CH3:14])[C:3]([C:5]1[CH:9]=[N:8][N:7]([CH3:10])[C:6]=1[C:11]([OH:13])=[O:12])=[O:4].N1(C(C2C=NN(C)C=2)=O)CC[CH2:16]1>>[N:2]1([C:3]([C:5]2[CH:9]=[N:8][N:7]([CH3:10])[C:6]=2[C:11]([OH:13])=[O:12])=[O:4])[CH2:14][CH2:16][CH2:1]1

Participants

3

Reactant 2

HCID 19623797HCID 19623797, compoundHCID 58446814Azetidin-1-yl-(1-methyl-1H-pyrazol-4-yl)-methanone

Product 1

HCID 58446922HCID 58446922, compound

Procedure

This compound was prepared in analogy to 4-dimethylcarbamoyl-2-methyl-2H-pyrazole-3-carboxylic acid (Example 97, step b) from azetidin-1-yl-(1-methyl-1H-pyrazol-4-yl)-methanone (500 mg, 3.33 mmol). Yield: 548 mg (81%); light red solid; MS: m/z=210.1 ([M+H]+).

Sources & evidence

ORD record
ord-a1dc21fc35d04438bd63f226104abab9
Source dataset
uspto-grants-2013_01
Patent number
US08349824B2

Reaction notes

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