HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704623Generated: October 30, 2026
Dichloromethane → HCID 20072898, compound
https://huagongshe.com/reaction/704623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 20072840 | HCID 20072840 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20072898 | HCID 20072898 | 29.1% |
Reaction Steps
To a suspension of methyl 7-carbamoylimidazo[1,2-a]-pyridine-2-carboxylate (1.5 g), methylene chloride (30 ml) and pyridine (2.7 g) was dropwise added trifluoroacetic anhydride (3.6 g) over the period of 5 minutes under cooling with stirring, and the mixture was stirred for 30 minutes at the same temperature. The reaction mixture was poured into ice water (30 ml) and extracted with 5% solution of methanol in chloroform. The organic layer was dried over magnesium sulfate and concentrated. The residue was subjected to a column chromatography on silica gel (50 g) and eluted with 20% solution of methanol in chloroform. The fractions containing the object compound were combined and concentrated to give methyl 7-cyanoimidazo[1,2-a]pyridine-2-carboxylate (0.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988698 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-c9148af8aeb84fa686a6b7f192119cac |
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| Source note | uspto-grants-1991_01 |
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