HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713154Generated: November 1, 2026
Sodium Carbonate → 5-[2-(4-Cyclobutylpiperazin-1-Yl)-2-Oxoethyl]-2-[3-(Methylsulfonyl)Phenyl]-4,5,6,7-Tetrahydro[1,3]Thiazolo[5,4-C]Pyridine
https://huagongshe.com/reaction/1713154
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-(Methylsulfonyl)phenylboronic acid | HCID 2773542 | — |
| Reactant | 2-Bromo-5-[2-(4-cyclobutylpiperazin-1-yl)-2-oxoethyl]-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine | HCID 57420586 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 5-[2-(4-Cyclobutylpiperazin-1-Yl)-2-Oxoethyl]-2-[3-(Methylsulfonyl)Phenyl]-4,5,6,7-Tetrahydro[1,3]Thiazolo[5,4-C]Pyridine | HCID 57420626 | — |
Reaction Steps
A mixture of 2-bromo-5-[2-(4-cyclobutylpiperazin-1-yl)-2-oxoethyl]-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine (40 mg, 0.1 mmol), 3-methylsulfonyl-phenylboronic acid (40 mg, 0.2 mmol), Na2CO3 (42 mg, 0.4 mmol) and Pd(PPh3)4 (12 mg, 0.01 mmol) in DME (4 mL) and water (1 mL) is degassed with argon and heated at 110° C. in a sealed tube overnight. The mixture is cooled and the layers are separated. The aqueous layer is extracted with EtOAc (4 ml) and the combined extracts are dried and evaporated. The residue is purified by PTLC to give the title compound as a white solid. MS (M+1): 475.0; 1H NMR (δ, CDCl3): 8.44 (t, 1H), 8.15 (td, 1H), 7.94 (td, 1H), 7.62 (t, 1H), 3.86 (s, 2H), 3.65 (q, 4H), 3.46 (d, 2H), 3.09 (s, 2H), 2.97 (s, 3H), 2.68-2.78 (m, 1H), 2.33 (q, 4H), 1.62-2.07 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795262B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-390a2a4708d147d088841cf2f40a21c5 |
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| Source note | uspto-grants-2010_09 |
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