HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275778Generated: October 31, 2026
Ethyl (chloroformyl)acetate → HCID 86717889, compound
https://huagongshe.com/reaction/2275778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl (chloroformyl)acetate | HCID 118030 | — |
| Reactant | 3-(2,6-Difluoro-benzyloxy)-pyridin-2-ylamine | HCID 10263498 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86717889 | HCID 86717889 | — |
Reaction Steps
1.93 g of 3-[(2,6-difluorobenzyl)oxy]pyridine-2-amine (Example 1A; 8.2 mmol, 1 equivalent) were initially charged in 50 ml of ethanol, and 8.2 g of ethyl 2-chloro-3-oxopropanoate (75% pure, crude product from Example 26A, 40.8 mmol, 5 equivalents) were added. The reaction mixture was heated at reflux overnight. The mixture was then concentrated under reduced pressure and the crude product obtained was chromatographed on 340 g of silica gel (Biotage Isolera) (mobile phase: cyclohexane:ethyl acetate gradient; Rf value of the product in cyclohexane:ethyl acetate 2:1=0.36). The product fractions were combined and concentrated and the residue obtained was triturated with diisopropyl ether. The solid was filtered off and dried under high vacuum. This gave 2.02 g of the title compound (71% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126998B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-05d6a94b510243a0a46172869e5964ac |
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| Source note | uspto-grants-2015_09 |
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