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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222366Generated: October 26, 2026

Triethylamine → Ethyl 2-[({1-[(3,4-dichlorophenyl)methyl]-5-methyl-1h-1,2,3-triazol-4-yl}carbonyl)amino]-1,3-oxazole-5-carboxylate

https://huagongshe.com/reaction/222366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantEthyl 2-amino-1,3-oxazole-5-carboxylateHCID 5260193—
Reactant1-(3,4-dichlorobenzyl)-5-methyl-1H-1,2,3-triazole-4-carboxylic acidHCID 55029873—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-[({1-[(3,4-dichlorophenyl)methyl]-5-methyl-1h-1,2,3-triazol-4-yl}carbonyl)amino]-1,3-oxazole-5-carboxylateHCID 59583669—

Reaction Steps

A mixture of 1-[(3,4-dichlorophenyl)methyl]-5-methyl-1H-1,2,3-triazole-4-carboxylic acid (Intermediate 4) (1 g, 3.4 mmol), ethyl 2-amino-1,3-oxazole-5-carboxylate (0.82 g, 5.2 mmol), HOBt (0.708 g, 5.2 mmol), EDCI (1.005 g, 5.2 mmol) and NEt3 (730 μL, 5.2 mmol) in DMF (50 mL) was stirred at room temperature for 2 days. The reaction was not completed and 2.5 eq of EDCI and HOBt were added and the reaction was heated at 40° C. and stirred for a further 14 days. Again no completed reaction was obtained. The solvent was evaporated and the residue was washed with water and extracted with DCM. The organic phase was dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography eluting with DCM/MeOH (90/10) to give after crystallisation from diisopropyl ether, the title compound as a yellow solid (98 mg, 6%). LC/MS: m/z 424 (M+H)+. Rt: 3.17 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207204B2
Source datasetuspto-grants-2012_06
ORD IDord-1460b74d06634048a94326d0f558edc7
Source noteuspto-grants-2012_06