HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844139Generated: November 2, 2026
Dimethyl Sulfoxide → HCID 86717887, compound
https://huagongshe.com/reaction/1844139
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-(2,6-Difluoro-benzyloxy)-pyridin-2-ylamine | HCID 10263498 | — |
| Reactant | Ethyl 2-chloro-3-cyclopropyl-3-oxopropanoate | HCID 54244501 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86717887 | HCID 86717887 | — |
Reaction Steps
1.69 g of 3-[(2,6-difluorobenzyl)oxy]pyridine-2-amine (Example 4A; 7.13 mmol, 1 equivalent) were initially charged in 44.4 ml of ethanol, and 425 mg of powdered molecular sieve 3 Å and 6.8 g of ethyl 2-chloro-3-cyclopropyl-3-oxopropanoate (crude product from Example 26A) were added. The resulting reaction mixture was heated at reflux for 48 h and then concentrated, and the residue was chromatographed (cyclohexane/ethyl acetate as mobile phase). The product-containing fractions were combined and concentrated under reduced pressure. The residue obtained in this manner was taken up in methanol, dimethyl sulphoxide and water and the solid formed was filtered off and dried under high vacuum. This gave 410 mg (15.4% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946215B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-ad8af143d26f4d24bbf340b57063b882 |
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| Source note | uspto-grants-2015_02 |
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