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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359659Generated: October 26, 2026

Diisopropylethylamine → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-methyl-5-phenyl-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/1359659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(R)-(+)-3-Aminoquinuclidine DihydrochlorideHCID 12494972—
Reactant1-methyl-5-phenyl-1H-pyrrole-2-carboxylic acidHCID 22350700—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-methyl-5-phenyl-1H-pyrrole-2-carboxamideHCID 981514731.1%

Reaction Steps

To a solution of (R)-(+)-3-aminoquinuclidine dihydrochloride (0.831 g, 4.17 mmol) in 55 mL of dry THF is added DIEA (2.08 mL, 11.9 mmol). After allowing the mixture to stir under nitrogen for 15 min, the product from Step 152c (0.800 g, X 3.98 mmol) is added. The mixture is allowed to stir for another 15 min, cooled in an A ice bath, and HATU (1.59 g, 4.17 mmol) is added. The reaction mixture is stirred on >an ice bath for 0.5 h, then at rt for an additional 2 h. The mixture is diluted with 60 mL CH2Cl2, washed with 50 mL of 1N NaOH and 50 mL of satd NaHCO3 solution, dried over MgSO4, filtered, and concentrated in vacuo. The crude product is purified by flash column chromatography (10% EtOAc, 1% NH4OH in CH2Cl2) to give 0.383 grams of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-methyl-5-phenyl-1H-pyrrole-2-carboxamide (31%) as a white solid. MS for C19H23N3O (ESI) (M+H)+ m/z 310.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599916B2
Source datasetuspto-grants-2003_07
ORD IDord-ff51a74cfd0340758f32cc40527a5b84
Source noteuspto-grants-2003_07