HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347721Generated: October 30, 2026
Dimethylformamide → HCID 58801101, compound
https://huagongshe.com/reaction/347721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | Methyl 2-(S)-[N-carbobenzyloxy]amino-3-aminopropionate, hydrochloride | HCID 13756825 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58801101 | HCID 58801101 | — |
Reaction Steps
To a solution of the compound of Reference Example 13 (300 mg) and ethyldiisopropylamine (0.656 ml) in dichloromethane (10 ml) is added chloroformic acid p-nitrophenyl ester (273 mg), and the mixture is stirred at 25° C. for 6 hours. To the reaction solution are added a solution of (2S)-3-amino-2-(benzyloxycarbonylamino)propanoic acid methyl ester hydrochloride (709 mg) and ethyldiisopropylamine (0.65 ml) in dimethylformamide (20 ml), and the mixture is stirred at 60° C. overnight. The reaction solution is diluted with ethyl acetate, and then the mixture is washed successively with 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate solution, and saturated brine, dried over magnesium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: gradient, 0% to 100% ethyl acetate/hexane) to give the title compound (120 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176199B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-7c41607a6f0b49038136f0efa8933284 |
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| Source note | uspto-grants-2007_02 |
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