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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224797Generated: October 31, 2026

Aniline → HCID 57125042, compound

https://huagongshe.com/reaction/224797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant4-ChloroanilineHCID 7812—
ReactantEthyl 6-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidine-3-carboxylateHCID 208414—
ReactantEthyl 7-methyl-4-oxo-6,7,8,9-tetrahydropyrido[1,2-a]pyrimidine-3-carboxylateHCID 15570105—
ProductHCID 57125042HCID 5712504260.2%

Reaction Steps

The process according to Example 6 is carried out except that p-chloro-aniline is replaced by aniline and ethyl-6-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido(1,2-a)pyrimidine-3-carboxylate is replaced by ethyl-7-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido(1,2-a)pyrimidine-3-carboxylate, respectively. Thus ethyl-9-(phenyl-hydrazono)-7-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido(1,2-a)pyrimidine-3-carboxylate is obtained with a yield of 60.2%. Mp.: 165°-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04234586
Source datasetuspto-grants-1980_11
ORD IDord-3dc8f4a979004b9a81330c59d4f82c21
Source noteuspto-grants-1980_11