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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12947Generated: October 27, 2026

(3aR,6aR)-1-(4'-Cyano-biphenyl-4-yl)-hexahydro-pyrrolo[3,4-b]pyrrole-5-carboxylic acid benzyl ester → HCID 44221502, compound

https://huagongshe.com/reaction/12947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3aR,6aR)-1-(4'-Cyano-biphenyl-4-yl)-hexahydro-pyrrolo[3,4-b]pyrrole-5-carboxylic acid benzyl esterHCID 44221920—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 44221502HCID 4422150264.4%

Reaction Steps

The product of Example 1D ((3aR,6aR)-1-(4′-Cyano-biphenyl-4-yl)-hexahydro-pyrrolo[3,4-b]pyrrole-5-carboxylic acid benzyl ester) (750 mg, 1.77 mmole) was refluxed in 10 ml trifluoroacetic acid for 2.5 hours. The solution was concentrated and triturated with dichloromethane. The residue was redissolved in dichloromethane and stirred with sodium bicarbonate powder. The solution was loaded on a silica gel column and purified by chromatography (0.6% ammonium hydroxide and 6% methanol in dichloromethane) to provide the title compound (330 mg, 64%), 1H NMR (CDCl3) δ ppm 7.64 (d, J=2.71 Hz, 4H) 7.51 (d, J=8.81 Hz, 2H) 6.66 (d, J=8.82 Hz, 2H) 4.07-4.17 (m, 1H) 3.50-3.65 (m, 1H) 3.24-3.36 (m, 1H) 2.86-3.10 (m, 5H) 2.15-2.29 (m, 1H) 1.74-1.93 (m, 1H). MS: (M+H)+=290.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728031B2
Source datasetuspto-grants-2010_06
ORD IDord-90e1a3312a3c43bbb73300a5d2126662
Source noteuspto-grants-2010_06