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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159019Generated: October 31, 2026

Aniline → HCID 68689719, compound

https://huagongshe.com/reaction/1159019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 16115648HCID 16115648—
ReactantSodium t-butoxideHCID 23676156—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventTolueneHCID 1140—
ProductHCID 68689719HCID 6868971955%

Reaction Steps

To a degassed solution of tris(dibenzylideneacetone) dipalladium(0) (7 mg, 0.007 mmol) and 2-(di-tert-butylphosphino)biphenyl (6 mg, 0.021 mmol) in toluene (2 mL) was added N-(t-butoxycarbonyl)-(R)-1,3,4,10b-tetrahydro-9-bromo-7-trifluoromethyl-pyrazino[2,1-a]isoindol-6(2H)-one (50 mg, 0.115 mmol). The mixture was degassed (alternating vacuum and argon) and aniline (0.031 mL, 0.345 mmol) and sodium tert-butoxide (33 mg, 0.345 mmol) were added. The mixture was degassed a final time and then subjected to microwave conditions (150° C., 1800 sec). The mixture was diluted with saturated aqueous sodium chloride and ethyl acetate, and the layers were separated. The aqueous layer washed with ethyl acetate (×2) and the combined organic layers were dried over sodium sulfate, filtered, and concentrated. The resulting residue was purified by radial chromatography (10-20% ethyl acetate in hexanes) to give 28 mg (55%) of a pale yellow residue. MS (ESI) 448 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812024B2
Source datasetuspto-grants-2010_10
ORD IDord-3f69aea413314a59a65649dac8d0c1f1
Source noteuspto-grants-2010_10