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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759573Generated: October 31, 2026

Methyl iodide → HCID 131712642, compound

https://huagongshe.com/reaction/1759573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 70547666HCID 70547666—
ProductHCID 131712642HCID 13171264259.9%

Reaction Steps

2-trans-(2-phenyl-ethenyl)-3-methyl-6,7-methylen-4-oxo-4H-pyrido[1,2-a]pyrimidine-7-carboxylic acid (0.8 g) was reacted with methyl iodide (0.55 g) and anhydrous K2CO3 (0.65 g) in dmethylformamide (7 ml) under stirring at room temperature for 4 hours. After dilution with ice water the precipitate was filtered off: crystallization from acetone gave 0.5 g of 2-trans-(2-phenyl-ethenyl)-3-methyl-6,7-methylen-4-oxo-4H-pyrido[1,2-a]pyrimidine-7-carboxylic acid, methyl ester, m.p. 164°-165° C. By proceeding analogously the following compound were prepared:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04341780
Source datasetuspto-grants-1982_07
ORD IDord-d6de7b3843ff4aef83b5edeea3c1ef36
Source noteuspto-grants-1982_07