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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868493Generated: November 3, 2026

Dimethylformamide → HCID 68513610, compound

https://huagongshe.com/reaction/1868493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 63701856HCID 63701856—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 68513610HCID 68513610—

Reaction Steps

3,4-Epoxypyrrolidine carbamate Wang resin (0.15 g, 0.18 mmol) was placed in a glass reaction vessel (4 mL). LiClO4 (57 mg, 3 eq.), N-Boc piperazine (186 mg, 5.5 eq.) and acetonitrile (2 mL) were added. The glass reactor was closed with a screw cap and the reaction mixture was heated at 80° C. for 43 h. The resin was transferred into syringes and washed with acetonitrile: H2O (1:1, 2×), DMF (3×), MeOH (3×), DMF (3×), and CH2Cl2 (5×). The BOC group was removed by treating the resin with 10% methyl sulfide in TFA (2 mL) for 1 hour. This solution was saved and later combined with a cleavage solution. The product was further cleaved from resin by shaking with a solution of TFA:CH2Cl2:H2O (2 mL of 70:30:1.5) for 2.5 h (2×). All the solutions were combined and condensed to afford 170 mg of crude 4-piperazin-1-yl-pyrrolidin-3-ol (bistrifluoroacetate salt, used without purification). The crude 4-piperazin-1-yl-pyrrolidin-3-ol was dissolved in DMF (dry, 2 mL). To this solution was added 4-chloro-benzoyl chloride (46 μL, 0.36 mmol), diisopropyl ethyl amine (620 μL, 3.6 mmol), and DMAP (2 mg). The solution was stirred at RT for 30 minutes, and then separated by preparative LC-MS to yield 16-mg of the title compound as the trifluoroacetate salt. ESIMS ([M+H]+): 448.3 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635698B2
Source datasetuspto-grants-2009_12
ORD IDord-92e0bffbf1784c3c8a2382e1375a7da5
Source noteuspto-grants-2009_12