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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16751Generated: October 24, 2026

Potassium Hydroxide → Tert-butyl 5-amino-3-[(3,5-dimethoxyphenyl)methoxy]pyrazole-1-carboxylate

https://huagongshe.com/en/reaction/16751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amineHCID 57440381—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 5-amino-3-[(3,5-dimethoxyphenyl)methoxy]pyrazole-1-carboxylateHCID 6658974199%

Reaction Steps

Potassium hydroxide (11.19 g, 199.4 mmol) dissolved in water (44.8 ml) was added to a solution of 5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine (7.121 g) dissolved in dichloromethane (40 ml). (2-Methylpropan-2-yl)oxycarbonyl tert-butyl carbonate (6.8 g, 31.2 mmol) dissolved in DCM (35 ml) was added and the reaction mixture was stirred vigorously at room temperature for 4 h. The reaction mixture was separated and the organic layer was washed with water (2×15 ml), brine (2×15 ml), dried over sodium sulphate, filtered, evaporated and dried in vacuo to give tert-butyl 5-amino-3-[(3,5-dimethoxyphenyl)methoxy]pyrazole-1-carboxylate (8.70 g, 99%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737149B2
Source datasetuspto-grants-2010_06
ORD IDord-4cf83e5733c04d5ea4181ad37e77c6c7
Source noteuspto-grants-2010_06