HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433666Generated: October 28, 2026
Triethylamine → 2-Tert-butoxycarbonylamino-3-[3-(1-{[4-(3-o-tolyl-ureido)-phenyl]-acetyl}-pyrrolidin-2-yl)-isoxazol-5-yl]-propionic acid methyl ester
https://huagongshe.com/reaction/433666
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 2-[(tert-butoxycarbonyl)amino]pent-4-ynoate | HCID 10537281 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | 1-(4-{2-[2-(Hydroxyimino-methyl)-pyrrolidin-1-yl]-2-oxo-ethyl}-phenyl)-3-o-tolyl-urea | HCID 87972858 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Tert-butoxycarbonylamino-3-[3-(1-{[4-(3-o-tolyl-ureido)-phenyl]-acetyl}-pyrrolidin-2-yl)-isoxazol-5-yl]-propionic acid methyl ester | HCID 20610304 | 14% |
Reaction Steps
A solution of 1-(4-{2-[2-(hydroxyimino-methyl)-pyrrolidin-1-yl]-2-oxo-ethyl}-phenyl)-3-o-tolyl-urea (300 mg, 0.789 mmol), 2-tert-butoxycarbonylamino-pent-4-ynoic acid methyl ester (359 mg, 1.182 mmol, crude mixture) and triethyl amine (12.9 μL) in dichloromethane (2 mL) was stirred 5 minutes. A sodium hypochlorite solution (5.25%, 2 mL) was added. The reaction was stirred at room temperature overnight. The aqueous portion was extracted 4 times with dichloromethane. The combined organic portions were washed with brine, dried over magnesium sulfate and concentrated. Chromatography of the crude mixture on a Biotage Flash 40S column eluting with ethyl acetate/hexane 1:5 gave the title compound (66 mg, 14%). MS (CI) m/z 604.5 (M−1), 505.9 (M-99)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06667331B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-5fe9ca639e4f4fc382497bdf18fb5f5c |
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| Source note | uspto-grants-2003_12 |
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