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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400944Generated: October 30, 2026

Triethylamine → (7-Chlorothieno[3,2-b]pyridin-2-yl)(4-methylpiperazin-1-yl)methanone

https://huagongshe.com/reaction/1400944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-MethylpiperazineHCID 53167—
Reactant7-Chlorothieno[3,2-b]pyridine-2-carbonyl chlorideHCID 22143543—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(7-Chlorothieno[3,2-b]pyridin-2-yl)(4-methylpiperazin-1-yl)methanoneHCID 5847474191.2%

Reaction Steps

1-Methylpiperazine (0.574 mL, 5.17 mmol) was added to a suspension of 7-chlorothieno[3,2-b]pyridine-2-carbonyl chloride (435, 1 g, 4.31 mmol) and Et3N (1.80 mL, 12.93 mmol) in DCM (50 mL). The reaction mixture was stirred for 1 h at room temperature, diluted with water and a saturated aqueous solution of ammonium chloride and extracted with DCM. The organic layer was successively washed with a saturated aqueous solution of ammonium chloride and brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by biotage (SNAP 25 g cartridge; MeOH/DCM: 0/100 to 10/90 over 20CV), to afford the title compound 436 (1.16 g, 3.93 mmol, 91% yield) as a yellow solid. MS (m/z): 296.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906852B2
Source datasetuspto-grants-2014_12
ORD IDord-c5c8457b7699425abb27e76defb3ada6
Source noteuspto-grants-2014_12