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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870964Generated: October 30, 2026

Cesium carbonate → HCID 86724450, compound

https://huagongshe.com/reaction/870964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBoc-L-leucinolHCID 7018766—
ReactantHCID 86695952HCID 86695952—
Catalystpalladium(II) acetateHCID 167845—
CatalystHCID 67346612HCID 67346612—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 86724450HCID 86724450187.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 8-chloro-4-methyl-5H-chromeno[3,4-c]pyridine (60 mg, 0.259 mmol), (S)-(−)-2-(tert-butoxycarbonylamino)-4-methyl-1-pentanol (113 mg, 0.518 mmol), 2-di-t-butylphosphino-2′,4′,6′-tri-1-propyl-1,1′-biphenyl (6.60 mg, 0.016 mmol), Cs2CO3 (127 mg, 0.388 mmol) and Pd(OAc)2 (1.744 mg, 7.77 μmol) in toluene (5 mL) was heated at 80° C. for 16 h. After cooling to rt, the mixture was diluted with EtOAc (10 mL) and water (10 mL). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to afford (S)-tert-butyl (4-methyl-1-((4-methyl-5H-chromeno[3,4-c]pyridin-8-yl)oxy)pentan-2-yl)carbamate, (0.2 g, 0.485 mmol, 30% yield) as a yellow solid. LCMS (ESI) m/e 413.39 [(M+H)+, calcd for C24H33N2O4 413.24]; LC/MS retention time (Method F): tR=0.97 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969564B2
Source datasetuspto-grants-2015_03
ORD IDord-fad848ec65774a1d864e35636cb27a1e
Source noteuspto-grants-2015_03