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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016464Generated: October 30, 2026

Ethanol → HCID 69545617, compound

https://huagongshe.com/reaction/1016464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2,3-Dichlorobenzeneboronic acidHCID 2734661—
ReactantHCID 69545705HCID 69545705—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 69545617HCID 6954561760%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of cyclopentyl-[2-(3-iodo-2,5-dimethyl-pyrazolo[1,5-a]pyrimidin-7-ylamino)-ethyl]-carbamic acid tert-butyl ester (38 mg, 0.076 mmol) and 2,3-dichlorobenzeneboronic acid in toluene (0.5 mL)/ethanol (0.5 mL)/2 M aqueous sodium carbonate (0.22 mL) was degassed (3×) by alternately pulling a vacuum followed by repressurization with nitrogen. Tetrakis(triphenylphosphine)palladium (10 mg, 0.009 mmol) was added, and the mixture was degassed (3×) again. The mixture was stirred for 2.5 hours at 100° C., concentrated under reduced pressure, and then chromatographed (4:1 hexanes/ethyl acetate) to give the product as colorless oil (24 mg, 60%): +APcI MS (M+1)+ 518; 1H NMR (CDCl3) δ7.42 (dd, 1 H), 7.30 (dd, 1H), 7.22 (t, 1H), 5.84 (s, 1H ), 4.25-4.10 (br s, 1H), 3.49 (s, 4H), 2.44 (s, 3H), 2.32 (s, 3H), 1.52 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476038B1
Source datasetuspto-grants-2002_11
ORD IDord-6a9f84a68bea43d3abc73c033e6d3e2c
Source noteuspto-grants-2002_11