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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387018Generated: October 31, 2026

Pyrrolidine → 2-Dimethylamino-6-methoxybenzo[b]thiophen-3-yl 4-[(1-Pyrrolidinyl)methyl]phenyl Ketone

https://huagongshe.com/reaction/1387018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant4-(Chloromethyl)benzoyl chlorideHCID 70136—
ReactantBenzo[b]thiophen-2-amine, 6-methoxy-N,N-dimethyl-HCID 10512530—
SolventChlorobenzeneHCID 7964—
Product2-Dimethylamino-6-methoxybenzo[b]thiophen-3-yl 4-[(1-Pyrrolidinyl)methyl]phenyl KetoneHCID 2118270274%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(Chloromethyl)benzoyl chloride (105 mg, 0.558 mmol) was added to a stirred solution of 2-dimethylamino-6-methoxybenzo[b]thiophene (105 mg, 0.507 mmol) in chlorobenzene (1 mL) under nitrogen. The resultant mixture was heated in an oil bath at 110° C. for 2.5 h. The mixture was cooled to 0° C., treated with pyrrolidine (5 mL), then allowed to stir at room temperature for 2 h. After dilution with THF (20 mL), the mixture was washed with saturated aqueous NaHCO3 (5 mL). The organic layer was dried over MgSO4, filtered, concentrated, and chromatographed on silica [gradient 20-40% EtOAc in hexanes, then 0-10% EtOH/Et3N (2/1) in THF/hexanes (1/1)] to give 148 mg (74%) of the ketone as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-01d69db52bdf454d9401912001aada42
Source noteuspto-grants-2001_07