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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774719Generated: November 3, 2026

2-Bromoethanol → HCID 90220917, compound

https://huagongshe.com/reaction/1774719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 90226274HCID 90226274—
SolventAcetoneHCID 180—
ProductHCID 90220917HCID 90220917—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 282 (50 mg, 0.122 mmol) in acetone was added potassium carbonate (25 mg, 0.244 mmol) and 2-bromo ethanol (18.3 mg, 0.146 mmol) and stirred for 12 h at 60° C. The reaction was filtered through celite bed and washed with ethyl acetate. The organic layer was concentrated to get the crude, which was purified by neutral alumina and the compound was eluted at 2% methanol in chloroform as half white coloured solid 2-(4-(4-(3-(3,5-difluoro-2-methoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-pyrazol-1-yl)piperidin-1-yl)ethanol 347. 1HNMR (400 MHz, DMSO) δ: 12.04 (s, 1H), 8.54 (d, 1H), 8.31 (s, 1H), 8.18 (d, 1H), 7.93 (s, 1H), 7.81 (d, 1H), 7.22 (m, 2H), 4.39 (m, 1H), 4.10 (m, 1H), 4.00 (m, 1H), 3.60 (s, 3H), 3.50 (m, 2H), 2.96 (d, 2H), 2.42 (m, 2H), 2.13 (m, 2H), 1.99 (m, 3H), 1.16 (t, 1H) and MS ES+454.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260426B2
Source datasetuspto-grants-2016_02
ORD IDord-3ea82665782549bcb6b1914f2834e042
Source noteuspto-grants-2016_02