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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-Bromo-4-chlorothieno(3,2-c)pyridine | HCID 17750390 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Tert-butyl 4-(2-bromothieno[3,2-c]pyridin-4-yl)piperazine-1-carboxylate | HCID 67156988 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943639B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-f16eb97eb10f433d8398366f8bce1c3e |
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| Source note | uspto-grants-2011_05 |
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