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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046221Generated: October 31, 2026

Potassium Iodide → HCID 67976139, compound

https://huagongshe.com/reaction/2046221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant(R)-3,3-Dimethyl-2-aminobutaneHCID 5324845—
ReactantSodium t-butoxideHCID 23676156—
Reactantethyl 1-(2-bromoethyl)-3-(phenoxymethyl)-1H-pyrazole-5-carboxylateHCID 67974304—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 67976139HCID 67976139233.7%
ProductHCID 67991632HCID 67991632—

Reaction Conditions

Temperature90 °C

Reaction Steps

(R)-3,3-Dimethyl-2-aminobutane (0.37 g, 2.86 mmol) was added to a suspension of 2-(2-bromoethyl)-5-phenoxymethyl-2H-pyrazole-3-carboxylic acid ethyl ester (0.1 g, 0.28 mmol) and potassium iodide (9 mg, 0.056 mmol) in ACN (1 mL). The mixture was stirred at 90° C. for 20 hours. Sodium tert-butoxide (41 mg, 0.42 mmol) and DMF (1 mL) was added and the mixture was stirred at 130° C. for 20 minutes under microwave irradiation. The solvent was evaporated in vacuo. The crude product was washed with a 2N solution of HCl until pH 1 and extracted with AcOEt. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo to yield a 1:1 mixture (R)-5-phenoxymethyl-2-[2-(1,2,2-trimethyl-propylamino)-ethyl]-2H-pyrazole-3-carboxylic acid ethyl ester and (R)-5-phenoxymethyl-2-[2-(1,2,2-trimethyl-propylamino)-ethyl]-2H-pyrazole-3-carboxylic acid (113 mg, 57%) as a yellow oil which was used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592422B2
Source datasetuspto-grants-2013_11
ORD IDord-4e3feca790eb4caa95c275f0a27d50b1
Source noteuspto-grants-2013_11