HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191093Generated: November 1, 2026
Hydrochloric Acid → HCID 131730097, compound
https://huagongshe.com/reaction/2191093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | tert-butyl N-(pyrrolidin-3-yl)carbamate | HCID 2757234 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 87571193 | HCID 87571193 | — |
| Catalyst | 2-(2'-Di-tert-butylphosphine)biphenylpalladium(II) acetate | HCID 11982262 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 131730097 | HCID 131730097 | 38% |
Reaction Steps
A mixture of Example 360 (100 mg, 0.18 mmol), 3-(tert-butoxycarbonylamino)-pyrrolidine (66 mg, 0.35 mmol), potassium tert-butoxide (28 mg, 0.25 mmol) and acetato(2′-di-tert-butylphosphino-1,1′-biphenyl-2-yl)palladium(II) (20 mg, 0.043 mmol) in 1,4-dioxane (2.0 mL) was heated in a sealed tube at 100° C., under microwave irradiation, for 2 h. The solvent was removed in vacuo and the residue was purified by column chromatography (SiO2, 0-100% EtOAc/heptane). The obtained solid was taken up in DCM (10 mL), treated with a solution of HCl in Et2O (2M, 1.0 mL, 2.0 mmol) and stirred at room temperature for 18 h. The solvent was removed in vacuo and the residue was purified by column chromatography (0-20% MeOH/DCM) to give the title compound (36 mg, 38%) as an orange solid. δH (CD3OD) 8.89-8.77 (1H, m), 8.57-8.44 (1H, m), 8.22-8.09 (1H, m), 7.62-7.51 (1H, m), 7.38-7.20 (2H, m), 7.02 (1H, d, J 7.7 Hz), 4.22-4.08 (1H, m), 3.93-3.48 (8H, m), 3.27-3.05 (4H, m), 2.81 (2H, s), 2.68-2.45 (3H, m), 2.38-2.21 (1H, m), 1.08 (6H, s). LCMS (ES+) 503.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324204B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-4b5e6c2ad5bf4bfd8929b9b37284b596 |
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| Source note | uspto-grants-2012_12 |
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