HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432921Generated: November 1, 2026
Propargyl bromide → 2-Benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl ester
https://huagongshe.com/reaction/1432921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 3-amino-2-(phenylmethoxycarbonylamino)propanoate;hydrochloride | HCID 21584654 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl ester | HCID 54423640 | — |
Reaction Steps
Propargyl bromide (1.6 mL, 14.4 mmol) is added to a solution of 3-amino-2-benzyloxycarbonylamino-propionic acid methyl ester hydrochloride (4.0 g, 13.9 mmol) and triethylamine (4.1 mL, 29.4 mmol) in THF (46 mL). The resulting mixture is heated to 50° C. and stirred overnight then cooled to RT and concentrated in vacuo. The crude residue is diluted with methylene chloride, washed with saturated NaHCO3 and brine then the organic layer is dried over MgSO4, filtered and concentrated in vacuo. The crude material (4.0 g) is taken on to the subsequent step without further purification. 1H NMR (CDCl3, 300 MHz) δ7.25-7.30 (m, 5H), 5.75 (bs, 1H), 5.20 (s, 2H), 4.45 (bs, 1H), 3.80 (s, 3H), 3.75 (m, 1H), 3.31 (s, 2H), 3.08 (dd, 1H), 2.98 (dd, 1H), 2.20 (t, 1H). EI MS, [M+H]+=291.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-03b821690b30428bb9fe4c28ee0ed4d3 |
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| Source note | uspto-grants-2009_11 |
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