HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75804Generated: October 28, 2026
Triethylamine → HCID 67353219, compound
https://huagongshe.com/reaction/75804
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Methyl valinate hydrochloride | HCID 111190 | — |
| Reactant | 3-(4-(3-(2,6-Difluorophenyl)ureido)-3-methylphenyl)isoxazole-5-carboxylic acid | HCID 67352205 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67353219 | HCID 67353219 | — |
Reaction Steps
3-(4-(3-(2,6-difluorophenyl)ureido)-3-methylphenyl)isoxazole-5-carboxylic acid (1.0 equiv.) was dissolved in 25 ml of DMF, N,N′-dicyclocarbodiimide (1.2 equiv.) and 1-hydroxybenzotriazole (1.0 equiv.) was added and stirred at room temperature for 10 min. L-valine methyl ester hydrochloride (1.5 equiv.) was neutralized with triethylamine (1.5 equiv.) in 10 ml of DMF and was added to the above mixture and the resulting reaction mixture was stirred at room temperature for 48 hours. DMF was evaporated and then diluted with EtOAc. The organic layer was washed with water, brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was dissolved in a chloroform and methanol mixture, adsorbed on silica (100-200 mesh) and purified by flash chromatography on silica gel, and then eluted with 0-2% methanol in chloroform to obtain a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835428B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-059b072d8465424da4fda90939e44e03 |
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| Source note | uspto-grants-2014_09 |
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