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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708048Generated: October 30, 2026

Water → HCID 58204233, compound

https://huagongshe.com/reaction/708048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantPotassium AcetateHCID 517044—
Reactant2-Methylpyridine-3-boronic acidHCID 20111647—
ReactantHCID 58203842HCID 58203842—
CatalystHCID 178418397HCID 178418397—
ProductHCID 58204233HCID 58204233—

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 9-Chloro-2-(1-isopropyl-1H-imidazol-2-yl)-4,5-dihydro-6-oxa-1-thia-10-aza-benzo[e]azulene (63 mg, 0.18 mmol), Potassium acetate (60.2 mg, 0.613 mmol), 2-methylpyridine-3-boronic acid, (32.2 mg, 0.235 mmol) and Tetrakis(triphenylphosphine)palladium(0) (28 mg, 0.024 mmol) in Acetonitrile (2 mL, 30 mmol) and Water (2 mL, 100 mmol) was degassed. The reaction was heated in the microwave at 140° C. for 20 minutes. The reaction was cooled to r.t., then extract with ethyl acetate. The combined organics were concentrated and purified by reverse phase HPLC to give 304. MS: (ESI+)=403.1. 1H NMR (400 MHz, DMSO) δ 8.55-8.47 (m, 1H), 7.86 (d, J=7.7 Hz, 1H), 7.54 (d, J=8.3 Hz, 1H), 7.50-7.43 (m, 2H), 7.36 (dd, J=7.7, 4.9 Hz, 1H), 7.29 (s, 1H), 7.00 (s, 1H), 4.82 (dt, J=13.3, 6.5 Hz, 1H), 4.43 (t, J=4.6 Hz, 2H), 2.65 (s, 3H), 1.44 (d, J=6.6 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175009B2
Source datasetuspto-grants-2015_11
ORD IDord-ca573c3722cf4639933b960547a7d425
Source noteuspto-grants-2015_11