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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772161Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 123644455, compound

https://huagongshe.com/reaction/1772161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium AcetateHCID 517044—
ReactantBis(neopentyl glycolato)diboronHCID 2734316—
ReactantHCID 117902383HCID 117902383—
CatalystPalladium ChlorideHCID 24290—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventDichloromethaneHCID 6344—
ProductHCID 123644455HCID 123644455—

Reaction Conditions

Temperature80 °C

Reaction Steps

1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (0.41 g, 0.6 mmol) is added to a mixture of tert-butyl-N-{1-[(6-amino-4-bromopyridin-2-yl)carbamoyl]ethyl}-N-methyl-carbamate B1 (5.2 g, 11.2 mmol), bis(neopentyl glycolato)diboron (5.1 g, 22.4 mmol), KOAc (3.3 g, 33.6 mmol) and DMSO (20 ml) under argon atmosphere and the mixture is stirred at 80° C. for 5 h. The mixture is diluted with DCM and extracted with a saturated aqueous sodium hydrogencarbonate solution. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by RP HPLC. Yield: 3.2 g (85%). HPLC-MS: M+H=339; tR=0.51 min (Method—2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249151B2
Source datasetuspto-grants-2016_02
ORD IDord-984811661e6c492d8c8cfbbdccb2527d
Source noteuspto-grants-2016_02