Sodium Bicarbonate → HCID 178424697, compound

Reaction equation

Br[CH2:2][C:3]1[C:7]([Cl:8])=[C:6]([C:9]2[C:10]([CH3:19])=[CH:11][C:12]([CH3:18])=[C:13]([CH:17]=2)[C:14]([OH:16])=[O:15])[NH:5][N:4]=1.C([O-])(O)=[O:21].[Na+]>>[Cl:8][C:7]1[C:3]([CH2:2][OH:21])=[N:4][NH:5][C:6]=1[C:9]1[C:10]([CH3:19])=[CH:11][C:12]([CH3:18])=[C:13]([CH:17]=1)[C:14]([OH:16])=[O:15]

Participants

Reactant 2

HCID 516892Sodium Bicarbonate

HCID 178424692HCID 178424692, compound2×

Product 1

HCID 178424697HCID 178424697, compound

Procedure

A mixture of 5-(3-(bromomethyl)-4-chloro-1H-pyrazol-5-yl)-2,4-dimethylbenzoic acid (compound 304.1, 200 mg, 0.58 mmol) and NaHCO3 (0.3 M, 10 mL) was stirred for 30 min at room temperature, then concentrated under reduced pressure. This resulted in 200 ma (crude) of the title compound as a white solid.

Workup

concentrationconcentrated under reduced pressure

Sources & evidence

ORD record: ord-98563559d3474174ae80268accd53e01
Source dataset: uspto-grants-2016_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09428502B2

Reaction notes

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