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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833342Generated: October 30, 2026

Phosphorus oxychloride → 5-Chloro-2-methylpyrazolo[1,5-a]pyrido[3,4-e]pyrimidine

https://huagongshe.com/reaction/1833342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Methylpyrazolo[1,5-a]pyrido[3,4-e]pyrimidin-5(4H)-oneHCID 136142359—
Product5-Chloro-2-methylpyrazolo[1,5-a]pyrido[3,4-e]pyrimidineHCID 21389185—

Reaction Steps

200 g. of 2-methylpyrazolo[1,5-a]pyrido[3,4-e]-pyrimidin-5(4H)-one of Example 1c are refluxed with 800 ml. of phosphorus oxychloride overnight. The excess phosphorus oxychloride is removed in vacuo and the oily residue decomposed by pouring on ice. The acidic aqueous solution is made alkaline with sodium hydroxide. The precipitated 5-chloro-2-methylpyrazolo[1,5-a]pyrido[3,4-e]pyrimidine is filtered off, yield: 143 g. (66%); m.p. 169.8° (ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066645
Source datasetuspto-grants-1978_01
ORD IDord-17fc6805ef334857b62c9c421f655886
Source noteuspto-grants-1978_01