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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274861Generated: November 2, 2026

2-Thiophenecarboxaldehyde → HCID 73866026, compound

https://huagongshe.com/reaction/1274861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantPiperidineHCID 8082—
ReactantEthyl 4-(2,3-dihydro-6-methyl-4-oxo-5-phenyl-1,3-oxazin-3-yl)-4-methyl-3-oxo-pentanoateHCID 22118254—
SolventTolueneHCID 1140—
ProductHCID 73866026HCID 7386602631.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 4-(2,3-dihydro-6-methyl-5-phenyl-4-oxo4H-1,3-oxazin-3-yl)-4-methyl-3-oxo-pentanoate (0.50 g), 2-thiophenecarboxaldehyde(0.34 g), piperidine(0.43 g) and molecular sieve 4A in toluene was stirred at 80° C. for 7 hrs. The reaction solution was filtered (celite), evaporated and recrystallised (ethanol) to give ethyl 4-methyl-4-(2,3-dihydro-6-methyl-5-phenyl-4-oxo-4H-1,3-oxazin-3-yl)-2-(2-thienylmethylidene)-3-oxo-pentanoate (Compound 206, 0.20 g), NMR 1.23(t,3H) 1.58(s,6H) 1.94(s,3H) 4.29(q,2H) 5.19(s,2H) 7.05(7.20-7.37(6H) 7.48(1H) 8.05(s,1H). By proceeding in a similar manner the following compounds were also obtained:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159902
Source datasetuspto-grants-2000_12
ORD IDord-265e0beb230546fba16d6b744e9967a6
Source noteuspto-grants-2000_12