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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583338Generated: November 1, 2026

Ethyl 2-methylacetoacetate → HCID 13105849, compound

https://huagongshe.com/reaction/1583338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
Reactant2-AminothiazoleHCID 2155—
ProductHCID 13105849HCID 13105849—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-amino-thiazole (3.06 g) was reacted with ethyl 2-methylacetoacetate (6.4 g) in polyphosphoric acid (15.3 g: 7.1 g of P2O5 and 8.2 g of 99% H3PO4) under stirring at 100° C. for two hours. After cooling, dilution with ice water and neutralization, the precipitate was filtered, washed with water and crystallized from isopropyl ether to give 6,7-dimethyl-5H-thiazolo[3,2-a]pyrimidine-5-one, m.p. 112°-113° C. (5.04 g), which was reacted with 3-pyridine-carboxaldehyde (5.99 g) in methanol (130 ml) in the presence of sodium methoxide (4.55 g) under stirring at reflux temperature for 12 hours. After cooling the precipitate was filtered and washed with water until neutral: crystallization from methanol gave 3.2 g of 6-methyl-7-trans-[2-(3-pyridyl)-ethenyl]-5H-thiazolo[3,2-a]pyrimidine-5-one, m.p. 192°-194° C., NMR (CDCl3) δ ppm: 2.36 (s) (3H, CH3), 6.97 (d) (H, C-2 proton), 7.38 (dd) (1H, C-5 pyridyl proton), 7.38 (d) (1H, β-ethenyl proton), 7.91 (d) (1H, α-ethenyl proton), 7.97 (d) (1H, C-3 proton), 8.00 (m) (1H, C-4 pyridyl proton), 8.62 (dd) (1H, C-6 pyridyl proton), 8.88 (d) (1H, C-2 pyridyl proton); JHα Hβ =16 Hz.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551457
Source datasetuspto-grants-1985_11
ORD IDord-783f4e395693490c9b38dd25336fc617
Source noteuspto-grants-1985_11