Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873971Generated: October 26, 2026

Water → Benzyl 2-(1-benzyl-3-cyclopropylindazol-6-yloxy)ethylcarbamate

https://huagongshe.com/reaction/1873971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactantbenzyl N-(2-bromoethyl)carbamateHCID 278694—
Reactant1-Benzyl-3-cyclopropylindazol-6-olHCID 135869942—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 2-(1-benzyl-3-cyclopropylindazol-6-yloxy)ethylcarbamateHCID 59370774—

Reaction Conditions

Temperature50 °C

Reaction Steps

Benzyl 2-bromoethylcarbamate (1.0563 g) which can be prepared according to the method described in Reference example 40, etc. was dissolved in dehydrated DMF (5 mL), added with 1-benzyl-3-cyclopropylindazol-6-ol (533.4 mg) which can be prepared according to the method described in Reference example 3, etc. and potassium carbonate (879.1 mg), and stirred overnight at 50° C. under nitrogen atmosphere. After cooling to room temperature, the reaction solution was added to water and extraction was carried out twice with ethyl acetate. The organic layer was washed twice with water and once with brine and dried over sodium sulfate. After the solvent was evaporated under reduced pressure, the resulting reside was purified by column chromatography (“COLUMN-B”; n-hexane:ethyl acetate=81:19→60:40) to obtain the title compound as a crude product (508.2 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304443B2
Source datasetuspto-grants-2012_11
ORD IDord-cfac119e45ad4e9f8922ddc737d836a9
Source noteuspto-grants-2012_11