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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549290Generated: October 29, 2026

Potassium Carbonate → Tert-butyl 4-(2-bromothieno[3,2-c]pyridin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/549290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-Bromo-4-chlorothieno(3,2-c)pyridineHCID 17750390—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 4-(2-bromothieno[3,2-c]pyridin-4-yl)piperazine-1-carboxylateHCID 6715698825%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Bromo-4-chlorothieno[3,2-c]pyridine (5.0 g, 20.24 mmol) and K2CO3 (13.97 g, 101.2 mmol) was stirred in DMSO (20 mL) followed by addition of tert-butyl piperazine-1-carboxylate (4.14 g, 22.26 mmol). The reaction mixture was stirred at 100° C. for 6 days. The reaction mixture was filtered to eliminate the carbonate and addition of water (50 mL) and ethyl was followed. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried (MgSO4) and the solvent was evaporated. The crude product was purified by flash chromatography using ethyl acetate/hexanes (2/8) as eluent to give 2 g of the desired product, yield 25%, 99% pure. 1H NMR (270 MHz, CDCl3) δ 1.48 (s, 9H), 1.52-1.63 (m, 1H), 3.42-3.47 (m, 4H), 3.61-3.64 (m, 4H), 7.22 (dd, J=5.4, 1 Hz, 1H), 7.35 (d, J=1 Hz, 1H), 8.04 (d, J=5.4 Hz, 1H). m/z=398.91 (M+H), bromide pattern.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943639B2
Source datasetuspto-grants-2011_05
ORD IDord-f16eb97eb10f433d8398366f8bce1c3e
Source noteuspto-grants-2011_05