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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801674Generated: November 1, 2026

2-Thiophenecarboxaldehyde → HCID 67547935, compound

https://huagongshe.com/reaction/1801674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
Reactant3-bromo-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 291524—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 67547935HCID 67547935—

Reaction Steps

The title compound was prepared from 3-bromo-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (500 mg, 2.091 mmol) and thiophene-2-carboxaldehyde (351 mg, 3.129 mmol) in the presence of sodium ethoxide (284 mg, 4.175 mmol) in absolute ethanol (25 ml) as described in Intermediate 1 to give 283 mg of the product as a light yellow solid; 1H NMR (300 MHz, CDCl3) δ 7.06 (s, 2H), 7.31-7.43 (m, 3H), 7.63 (dd, J=2.4, 16.2 Hz, 2H), 8.15 (d, J=14.7 Hz, 1H), 8.94 (d, J=6.9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349846B2
Source datasetuspto-grants-2013_01
ORD IDord-f339d545e2a44b038c6c188670fb976b
Source noteuspto-grants-2013_01