HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977060Generated: October 30, 2026
Dichloromethane → HCID 19964159, compound
https://huagongshe.com/reaction/977060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-ethoxypyridin-3-amine | HCID 817252 | — |
| Reactant | HCID 15003653 | HCID 15003653 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 19964159 | HCID 19964159 | — |
Reaction Steps
2-Chlorosulfonyl-5-methoxy-7-methyl[1,2,4]triazolo[1,5-c]pyrimidine (1.5 g, 5.7 mmol) was added to a solution of 0.8 g (5.7 mmol) of 3-amino-4-ethoxypyridine in 30 mL of dry pyridine in portions over 10 minutes with stirring. After 16 hours the reaction mixture was poured into 400 mL of dichloromethane. The resulting mixture was washed with 150 mL of water, dried over magnesium smlfate, and filtered. The liltrate was combined with 5 g of silica gel and the mixture was concentrated by evaporation under reduced pressure. The resulting silica plug was placed onto a 200 g silica gel column and eluted with dichloromethane containing increasing amount of ethanol. The product fractions were combined and concentrated by evaporation under reduced pressure and the solid obtained was dried to obtain 0.75 g (36 percent of theory) of the title compound as a white solid melting at 184°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614469 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-e906353c02b447eb8df170b2dffed763 |
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| Source note | uspto-grants-1997_03 |
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