Ammonium Hydroxide → HCID 66958625, compound

Reaction equation

[CH2:1]([N:3]1[C:7]([CH2:8][CH2:9][S:10]([CH3:13])(=[O:12])=[O:11])=[CH:6][C:5]([C:14]([O:16]CC)=O)=[N:4]1)[CH3:2].[OH-].[NH4+:20]>>[CH2:1]([N:3]1[C:7]([CH2:8][CH2:9][S:10]([CH3:13])(=[O:12])=[O:11])=[CH:6][C:5]([C:14]([NH2:20])=[O:16])=[N:4]1)[CH3:2]

Participants

Reactant 2

HCID 14923Ammonium Hydroxide

HCID 66958712HCID 66958712, compound

Product 1

HCID 66958625HCID 66958625, compound

Procedure

The method described in Part C of Example 10 was used to treat ethyl 1-ethyl-5-(2-methanesulfonylethyl)-1H-pyrazole-3-carboxylate (4.6 g, 17 mmol) with ammonium hydroxide (100 mL). The solid was isolated by filtration and washed with water to provide 3.0 g of 1-ethyl-5-(2-methanesulfonylethyl)-1H-pyrazole-3-carboxamide as a white powder, which was mixed with material from another run.

Workup

customThe solid was isolated by filtration
washwashed with water

Sources & evidence

ORD record: ord-cf7a9dea088d4812b3676141ec7c74c2
Source dataset: uspto-grants-2011_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07879849B2

Reaction notes

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