HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447373Generated: October 30, 2026
Ethyl Acetate → (1R*,2S*)-2-(3-((E)-2-(pyridin-3-yl)vinyl)-1H-indazol-6-yl)spiro[cyclopropane-1,3'-indolin]-2'-one
https://huagongshe.com/reaction/447373
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-((E)-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)ethenyl)pyridine | HCID 57982716 | — |
| Reactant | HCID 178506567 | HCID 178506567 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1R*,2S*)-2-(3-((E)-2-(pyridin-3-yl)vinyl)-1H-indazol-6-yl)spiro[cyclopropane-1,3'-indolin]-2'-one | HCID 58486164 | 44% |
Reaction Steps
To a solution of (1R,2S)-2-(3-iodo-1H-indazol-spiro[cyclopropane-1,3′-indolin]-2′-one (50 mg, 0.12 mmol) in DMF (0.4 mL) and water (0.1 mL) was added (E)-3-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)pyridine (50 mg, 0.2 mmol) potassium fluoride (14 mg, 0.24 mmol) and Pd(PPh3)4 (7 mg, 0.006 mmol). The mixture was heated to 120° C. for 2 h under microwave irradiation. Ethyl acetate (50 mL) was added and the solution was washed with water (2×5 mL), brine (5 mL) and dried over MgSO4. Purification by reverse phase preparatory HPLC gave the title compound as a yellow solid (20 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481533B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-9940d84039804d64a22b95abad9f75b1 |
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| Source note | uspto-grants-2013_07 |
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