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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877958Generated: November 3, 2026

Sodium Carbonate → 5-(2-Thiophen-2-yl-phenyl)-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/1877958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactant5-(2-Bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridineHCID 58827122—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-(2-Thiophen-2-yl-phenyl)-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridineHCID 58827109—

Reaction Steps

To a solution of 5-(2-bromophenyl)-5,6,7,8,-tetrahydro-imidazo[1,5-a]pyridine, Example 12D (120 mg, 0.43 mmol) in DME (2 mL) is added thiophene-2-boronic acid (166 mg, 1.3 mmol), aqueous Na2CO3 (2M, 1.0 mL, 2.0 mmol), and Pd(PPh3)4 (20 mg). The reaction mixture is refluxed overnight. The mixture is partitioned between EtOAc and 1M NaOH. The organic layer is washed by sat. NaHCO3, dried and concentrated to give an oil. The crude reaction mixture is subjected to flash chromatography (silica gel) eluting with acetone:hexane to yield the desired compound. MS (ESI) m/z 280 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.58-1.74 (m, 1 H), 1.85-2.01 (m, 2 H), 2.14-2.27 (m, 1 H), 2.74-2.94 (m, 2 H), 5.45 (dd, J=8.6, 5.1 Hz, 1 H), 6.81 (s, 1 H), 7.00-7.05 (m, 2 H), 7.06 (s, 1 H), 7.10 (dd, J=5.3, 3.5 Hz, 1 H), 7.31-7.37 (m, 2 H), 7.39 (dd, J=5.2, 1.1 Hz, 1 H), 7.41-7.46 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-80a219c113a84b77ba7af52c6e9341dc
Source noteuspto-grants-2012_11