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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Ethyl 2-amino-1,3-oxazole-5-carboxylate | HCID 5260193 | — |
| Reactant | 1-(3,4-dichlorobenzyl)-5-methyl-1H-1,2,3-triazole-4-carboxylic acid | HCID 55029873 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-[({1-[(3,4-dichlorophenyl)methyl]-5-methyl-1h-1,2,3-triazol-4-yl}carbonyl)amino]-1,3-oxazole-5-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207204B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-1460b74d06634048a94326d0f558edc7 |
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| Source note | uspto-grants-2012_06 |
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