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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278598Generated: November 2, 2026

Acetic Acid → Dimethyl 4-(2,6-dichlorophenyl)-2-(2-methoxy-2-oxoethyl)-6-[2-(1,3-thiazol-2-yl)ethyl]-1,4-dihydropyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/1278598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-ButanolHCID 6386—
ReactantDimethyl 3-aminoglutaconateHCID 253819—
ReactantMethyl 3-(2,6-dichlorophenyl)-2-[(1,3-thiazol-2-yl)propanoyl]-2-propenoateHCID 69949834—
ReactantHCID 178461630HCID 178461630—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl 4-(2,6-dichlorophenyl)-2-(2-methoxy-2-oxoethyl)-6-[2-(1,3-thiazol-2-yl)ethyl]-1,4-dihydropyridine-3,5-dicarboxylateHCID 1016516085%

Reaction Steps

To a stirred solution of 2-methyl-2-propanol (92.8 g, 1252 mmol; 2.1 eq.) in anhydrous THF (1100 ml) was added a 1.0 M solution of EtMgBr in THF (1192 ml, 1192 mmol; 2.0 eq.) dropwise slowly at 0° C. under nitrogen atmosphere for 2 hours period. The resulting solution was stirred at room temperature for 1 hour. Then to the mixture was added a solution of dimethyl 3-amino-2-pentenedioate (113.5 g, 655 mmol; 1.1 eq.) in anhydrous THF (550 ml) dropwise slowly at 0° C. for 20 minutes. The resulting pale yellow solution was stirred at the same temperature for 1 h, then a solution of methyl 3-(2,6-dichlorophenyl)-2-[(1,3-thiazol-2-yl)propanoyl]-2-propenoate (219.9 g, 594 mmol; 1.0 eq.) in anhydrous THF (550 ml) was added at 0° C. for 30 minutes. The reaction mixture was stirred at room temperature for 16 hours under nitrogen atmosphere, then acetic acid (170 ml; 5.0 eq.) was added at 0° C. The resulting mixture was stirred at room temperature for 6 hours. The mixture was poured into 2 NNaOHaq. (1000 ml), the organic phase was separated and the aqueous phase was extracted with EtOAc (2000 ml). The combined organic phase was washed with H2O (1000 ml) and brine (1000 ml), dried (Na2SO4) and concentrated to give a crude mixture. Purification on silica gel column chromatography (3 times 1700 g) eluted with hexane/EtOAc (2/1 to 1/2) to afford 246.0 g (85% ) of dimethyl 4-(2,6-dichlorophenyl)-2-(2-methoxy-2-oxoethyl)-6-[2-(1,3-thiazol-2-yl)ethyl]-1,4-dihydropyridine-3,5-dicarboxylate as a brown oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444677B2
Source datasetuspto-grants-2002_09
ORD IDord-40a7b3c88302402fb8d2f5c61f1f1e5d
Source noteuspto-grants-2002_09