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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029914Generated: November 2, 2026

3-Pyridineacetic acid → HCID 67915794, compound

https://huagongshe.com/reaction/1029914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridineacetic acidHCID 108—
ReactantTriethylamineHCID 8471—
Reactant7,7-Diphenylhexahydro-1H-isoindol-4(2H)-one hydrochlorideHCID 21264543—
SolventDichloromethaneHCID 6344—
ProductHCID 67915794HCID 6791579444.9%

Reaction Steps

N,N'-Carbonyldiimidazole (0.81 g) is added to a solution of 2-(3-pyridyl)acetic acid (0.685 g) in dry dichloromethane (15 cc), cooled to +5° C. The mixture is stirred for 30 minutes at +5° C. and a solution of (3aRS,7aRS)-7,7-diphenyl-4-perhydroisoindolone hydrochloride (1.6 g) and triethylamine (0.7 cc) in dichloromethane (10 cc) is then added. The reaction mixture is stirred at 20° C. for 16 hours and then concentrated to dryness under reduced pressure (2.7 kPa). The residue is taken up in a mixture of ethyl acetate (100 cc) and water (75 cc). The organic phase is washed with saturated sodium chloride solution (50 cc), dried over magnesium sulphate and filtered and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a basic alumina column (diameter 2 cm, height 15 cm), eluting with ethyl acetate and collecting 50 cc fractions. Fractions 4 to 24 are concentrated to dryness under reduced pressure (2.7 kPa). The crystals obtained are recrystallized from acetonitrile (cc) to give (3aRS,7aRS)-7,7-diphenyl-2-[2-(3-pyridyl)acetyl]-4-perhydroisoindolone (0.9 g) in the form of white crystals melting at 208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102667
Source datasetuspto-grants-1992_04
ORD IDord-58b1d98392b5411ea19a61c5d0f5c027
Source noteuspto-grants-1992_04