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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478283Generated: November 1, 2026

Potassium Carbonate → HCID 86697449, compound

https://huagongshe.com/reaction/1478283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Methoxypyridin-3-yl)boronic acidHCID 2762709—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 86697447HCID 86697447—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 86697449HCID 8669744917.5%

Reaction Steps

(S)-2-amino-N—((S)-1-(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)pyrrolidin-3-yl)-N,4-dimethylpentanamide (220 mg, 0.54 mmol), 2-methoxypyridine-3-boronic acid (164 mg, 1.1 mmol), potassium carbonate (291 mg, 2.15 mmol), Pd(OAc)2 (2 mg, 0.011 mmol) and x-phos (10 mg, 0.022 mmol) were taken up in 2 mL acetonitrile and 1 mL water and heated in a sealed tube at 85° C. for 2 hours. Reaction was then filtered through celite with acetonitrile and DCM reduced in vacuo, then purified on Shimadzu neutral phase prep and product fractions lyophilized to get (S)-2-amino-N—((S)-1-(3-(2-methoxypyridin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)pyrrolidin-3-yl)-N,4-dimethylpentanamide 41.3 mg as 0.5 eq formic salt. 1H NMR (400 MHz, DMSO-d6) δ 8.87-8.97 (m, 1H), 8.72 (s, 1H), 8.50 (s, 1H), 8.30 (s, 1H), 7.96 (dd, J=2.02, 4.80 Hz, 1H), 7.00-7.11 (m, 1H), 6.51 (d, J=7.83 Hz, 1H), 4.00 (s, 3H), 3.48-3.64 (m, 1H), 3.43 (br. s., 3H), 2.96 (s, 2H), 2.81 (s, 1H), 2.11-2.28 (m, 2H), 1.72-1.89 (m, 1H), 1.19-1.39 (m, 2H), 0.90 (dd, J=1.89, 6.69 Hz, 6H). (ESI) m/z 438 [(M+H)]+, calc'd for C23H31N7O2: 437.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403832B2
Source datasetuspto-grants-2016_08
ORD IDord-e20451d429a34e8fbd18af5ddbdc100b
Source noteuspto-grants-2016_08