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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159040Generated: October 30, 2026

Water → HCID 68689588, compound

https://huagongshe.com/reaction/1159040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(Z)-Prop-1-en-1-ylboronic acidHCID 5355539—
ReactantHCID 16115648HCID 16115648—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68689588HCID 6868958888.3%

Reaction Steps

To a stirring degassed solution of N-(t-butoxycarbonyl)-(R)-1,3,4,10b-tetrahydro-9-bromo-7-trifluoromethyl-pyrazino[2,1-a]isoindol-6(2H)-one (54 mg, 0.12 mmol) in DME (1.2 mL) was added tetrakis(triphenylphosphine)palladium(0) (1.7 mg, 0.0015 mmol). After 15 min., cis-1-propenylboronic acid (31 mg, 0.37 mmol), potassium carbonate (17 mg, 0.12 mmol), and water (0.3 mL) were added. The reaction was heated to reflux for 3 h and then cooled to room temp. The reaction was diluted with brine and extracted with EtOAc (3×5 mL). The organic layers were combined, dried over Na2SO4, and conc. in vacuo to a yellow oil. The oil was purified by flash chromatography (silica gel, 0-50% EtOAc in hexanes) to give 42 mg of the desired product as a colorless oil. MS (ESI) 397 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812024B2
Source datasetuspto-grants-2010_10
ORD IDord-9e17236320dd4139a20939632b6beb02
Source noteuspto-grants-2010_10