HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416645Generated: October 29, 2026
Diisopropylethylamine → HCID 86759568, compound
https://huagongshe.com/reaction/2416645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Boc-3-(2-pyridyl)-Ala-OH | HCID 2734482 | — |
| Reactant | O-benzylglycine toluene-p-sulphonate | HCID 6451311 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86759568 | HCID 86759568 | 90.6% |
Reaction Steps
To a solution of (2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-pyridyl)propanoic acid (55.0 g), glycine benzyl ester tosylate (69.7 g), and diphenylphosphoryl azide (46.7 ml) in N,N-dimethylformamide (550 ml) was added dropwise N,N-diisopropylethylamine (75.6 ml) at 4° C. The mixture was warmed to room temperature and stirred for 3 hours. The resulting mixture was poured into ice-cold saturated aqueous sodium hydrogencarbonate solution (700 ml). The mixture was extracted twice with ethyl acetate (total 1.3 L) and washed successively with water (400 ml×2), saturated aqueous ammonium chloride solution (200 ml), aqueous sodium hydrogencarbonate solution (300 ml×2), and brine (40 ml). The organic layer was dried over anhydrous magnesium sulfate and concentrated to give the title compound (77.4 g) as pale brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825200B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-aee862d091884d789cd7a378dfc12955 |
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| Source note | uspto-grants-2004_11 |
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