HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624987Generated: October 26, 2026
Diisopropylethylamine → HCID 76282857, compound
https://huagongshe.com/reaction/624987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromo-1-ethylpyridinium tetrafluoroborate | HCID 2736300 | — |
| Reactant | 6-(Cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)picolinic acid | HCID 71087292 | — |
| Reactant | 1,1-Dioxo-1,3-thiazolidine-4-carboxamide hydrochloride | HCID 90203843 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 76282857 | HCID 76282857 | 21% |
Reaction Steps
A solution of 6-cyclopropylmethoxy-5-(3,3-difluoro-azetidin-1-yl)-pyridine-2-carboxylic acid (Example 1 b, 200 mg, 704 μmol), 1,1-dioxo-1,3-thiazolidine-4-carboxamide hydrochloride (Example 127 d, 169 mg, 844 μmol), 2-bromo-1-ethylpyridinium tetrafluoroborate (212 mg, 774 μmol) and DIEA (273 mg, 361 μL, 2.11 mmol) in THF (20 mL) was stirred for 24 h at ambient temperature. The solvent was removed under reduced pressure, ice/sat. aqueous NaHCO3 (75 mL) and EtOAc (75 mL) were added and the layers were separated. The aqueous layer was extracted with EtOAc (75 mL). The combined extracts were washed with ice/0.1N HCl (75 mL) and ice/brine (75 mL), dried over Na2SO4 and filtered. The solvent was removed under reduced pressure to give a yellow solid which was recrystallized from EtOAc (3 mL). The crude product was purified by chiral HPLC (Reprosil Chiral NR, EtOH/heptane 40%/60%) to give the title compound (63 mg, 21%) as colorless oil, MS (EI): m/e=431.3 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303012B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-7f8e88dfd0184b13b8ebf05618e6c3f3 |
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| Source note | uspto-grants-2016_04 |
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