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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056015Generated: October 31, 2026

2-Bromoethanol → HCID 22346783, compound

https://huagongshe.com/reaction/2056015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178508725HCID 178508725—
SolventDimethylformamideHCID 6228—
ProductHCID 22346783HCID 2234678373.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (5.00 g, 19.1 mmol) in DMF (40 mL) was added sodium hydride (60%, 1.53 g, 38.3 mmol) and the reaction mixture was stirred for 20 min. 2-Bromoethanol (1.50 mL, 21.1 mmol) was added and the reaction mixture was heated at 50° C. for 18 h. The reaction mixture was cooled to ambient temperature and concentrated to afford a brown sludge. Ice water (50 mL) was added and the resulting precipitate was collected by filtration, rinsed with water (50 mL) and ether (50 mL), and dried in vacuo to afford 2-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-1-ethanol as a beige solid (4.30 g, 14.1 mmol): 1H NMR (d6-DMSO, 400 MHz): δH 8.19 (1H, s), 4.84 (1H, t, J=5.8 Hz), 4.30 (1H, t, J=5.8 Hz), and 3.77 (2H, app q, J=5.6 Hz); RP-HPLC (Hypersil C18, 5 μm, 100 Å, 15 cm; 5%-100% acetonitrile—0.1 M ammonium acetate over 15 min, 1 mL/min). Rt 7.35 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332497B2
Source datasetuspto-grants-2008_02
ORD IDord-57da9ae9285c4ab69afdbd2fcc98bb11
Source noteuspto-grants-2008_02