HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185487Generated: October 30, 2026
1,2-Dichloroethane → 4-[2-((S)-2-Cyclobutylcarbamoyl-pyrrolidin-1-yl)-2-oxo-ethoxy]-7-methyl-quinoline-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1185487
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Pentafluorophenol | HCID 13041 | — |
| Reactant | (S)-Pyrrolidine-2-carboxylic acid cyclobutylamide trifluoroacetate | HCID 68599196 | — |
| Reactant | 4-Carboxymethoxy-7-methyl-quinoline-2-carboxylic acid ethyl ester | HCID 68601583 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[2-((S)-2-Cyclobutylcarbamoyl-pyrrolidin-1-yl)-2-oxo-ethoxy]-7-methyl-quinoline-2-carboxylic acid ethyl ester | HCID 68599442 | — |
Reaction Steps
To a solution of 2 g of 4-Carboxymethoxy-7-methyl-quinoline-2-carboxylic acid ethyl ester in 30 ml of DCM, 3.6 g of EDC, 3.4 g of pentafluorophenol, 2.2 g of NEM was added and the reaction mixture was stirred at RT for 2 h. Then, 5.3 g of (S)-Pyrrolidine-2-carboxylic acid cyclobutylamide trifluoroacetate and 2.1 g of NEM in 10 ml of DCM was added. After 16 h the reaction mixture was diluted with water and extracted with DCM (3×150 ml). The combined organic phases were dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was purified by chromatography on silica gel eluting with a gradient of n-heptane/ethyl acetate. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 2.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08669266B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-19ca049e7ebb4b1f8d352e89e599719b |
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| Source note | uspto-grants-2014_03 |
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