HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061893Generated: November 1, 2026
Potassium Carbonate → HCID 131729984, compound
https://huagongshe.com/reaction/2061893
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3R,4R)-3-Amino-1-Boc-4-hydroxypyrrolidine | HCID 11275699 | — |
| Reactant | (Z)-ethyl 3-(dimethylamino)-2-(2-fluoro-5-iodobenzoyl)acrylate | HCID 70809441 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131729984 | HCID 131729984 | 64% |
Reaction Steps
Trans-tert-butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate (500 mg, 2.47 mmol) was added to the solution of (Z)-ethyl 3-(dimethylamino)-2-(3-iodobenzoyl)acrylate (Intermediate 24, 0.34M, 6.7 mL, 2.25 mmol) and the mixture was heated at 50° C. for 3 hour. The solvent was removed in vacuo and the residue was dried in a vacuum oven for 1.5 hours. The residue was then dissolved in dimethyl formamide (5 mL) and potassium carbonate powder (435 mg, 3.15 mmol) was added. The reaction was heated at 70° C. for 3 h then cooled to room temperature. Water (30 mL) was added and the suspension was extracted with 1:1 ethyl acetate:methyl tert-butyl ether (3×50 mL). The organic layers were dried over sodium sulfate, and the solvent was removed in vacuo. The residue was suspended in methyl tert-butyl ether (20 mL) and stirred at 40° C. for 1 h. The suspension was filtered and the solid dried to give 751 mg (64% yield) of racemic trans-ethyl 1-(1-(tert-butoxycarbonyl)-4-hydroxypyrrolidin-3-yl)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate as a yellowish powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283361B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-1caa704022464a8fa77127924cc3669d |
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| Source note | uspto-grants-2012_10 |
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