HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58910Generated: October 28, 2026
Phenylacetyl chloride → (S)-Benzyl 2-((tert-butoxycarbonyl)amino)-3-(pyridin-2-yl)propanoate
https://huagongshe.com/reaction/58910
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Boc-3-(2-pyridyl)-Ala-OH | HCID 2734482 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-Benzyl 2-((tert-butoxycarbonyl)amino)-3-(pyridin-2-yl)propanoate | HCID 15172404 | 42% |
Reaction Steps
To (S)-2-((tert-butoxycarbonyl)amino)-3-(pyridin-2-yl)propanoic acid (1.00 g, 3.76 mmol) in DCM (10 mL) was added TEA (0.974 mL, 7.52 mmol) and DMAP (23 mg, 0.188 mmol) and the reaction mixture was cooled to 0° C. and BnCOCl (635 mL, 4.51 mmol) was added via an addition funnel over 20 min. The mixture was allowed to warm to ambient temperature overnight at which time it was quenched with sodium bicarbonate (sat.), extracted with ethyl acetate (2×), dried with sodium sulfate, filtered, and concentrated. Purification by column chromatography (0-50% ethyl acetate/hexanes+1% TEA) provided (S)-benzyl 2-((tert-butoxycarbonyl)amino)-3-(pyridin-2-yl)propanoate (0.558 g, 42%) as a light brown solid. MS (EI) for C20H24N2O4, found 257.2 [M-Boc]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434761B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-30105b5f79f64bea92fe676233482da6 |
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| Source note | uspto-grants-2016_09 |
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