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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256309Generated: October 30, 2026

1,4-Dioxane → HCID 67064496, compound

https://huagongshe.com/reaction/1256309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantN-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamideHCID 86652272—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventMethanolHCID 887—
ProductHCID 67064496HCID 6706449627%

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2D, 50 mg, 151 mmol), 3-dihydrobenzofuran-5-ylboronic acid (50 mg, 305 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (9 mg, 12 mmol) in 2:1 1,4-dioxane/saturated aqueous NaHCO3 (670 microliters of 1,4-dioxane and 330 microliters of saturated aqueous NaHCO3) was prepared in a 2 mL microwave reaction vessel and the sealed reaction vessel warmed to 110° C. for 20 minutes. The reaction mixture was cooled to rt, diluted with methanol, filtered, and purified via preparative HPLC, 45-70% (MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a yellow solid (16.8 mg, 27%). Melting point (174.2.0-184.3° C.). 1HNMR (400 MHz, DMSO-d6) δ ppm 1.46 (s, 6 H) 3.32 (t, J=8.59 Hz, 2 H) 4.67 (t, J=8.72 Hz, 2 H) 6.56 (d, J=2.27 Hz, 1 H) 7.01 (d, J=8.59 Hz, 1 H) 7.62 (d, J=8.34 Hz, 2 H) 7.95 (dd, J=8.46, 1.64 Hz, 1 H) 8.00-8.08 (m, 4 H) 8.19 (d, J=2.02 Hz, 1 H) 11.20 (s, 1 H). ESI-MS: m/z 415.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461163B2
Source datasetuspto-grants-2013_06
ORD IDord-900784e7eacf4dce871a1f9a96623c09
Source noteuspto-grants-2013_06