HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409932Generated: October 30, 2026
4-Methylmorpholine → 1-[4-(2-Carbamoylpyridin-4-yloxy)-2-fluorophenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester
https://huagongshe.com/reaction/409932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(Benzyloxycarbonyl)cyclopropanecarboxylic acid | HCID 57470860 | — |
| Reactant | 4-(4-Amino-3-fluorophenoxy)pyridine-2-carboxyamide | HCID 131731635 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[4-(2-Carbamoylpyridin-4-yloxy)-2-fluorophenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester | HCID 24788499 | — |
Reaction Steps
Thionyl chloride was added at −20° C. to a solution of 1-(benzyloxycarbonyl)cyclopropanecarboxylic acid (97.98 g) in tetrahydrofuran (200 ml) and N-methylpyrrolidone (200 ml) and stirred for 30 minutes. A solution of 4-(4-amino-3-fluorophenoxy)pyridine-2-carboxyamide (100 g) and N-methylmorpholine (40.91 g) in N-methylpyrrolidone (600 ml) were added to the reaction mixture at the same temperature and stirred for 1 hour at 10° C. Water (100 g) was added to the reaction mixture and stirred for 1 hour at 20° C. After confirming the crystal precipitation, a 1N sodium hydroxide aqueous solution (1 L) was added and further stirred for 19 hours. The precipitated solid was collected by filtration and washed with water (500 g). The obtained solid was dried for 20 hours at 60° C. to give 176.7 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759530B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f5229ec57e0440a398aace9b2b83cb4b |
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| Source note | uspto-grants-2014_06 |
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