HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278810Generated: November 3, 2026
Diisopropylethylamine → HCID 131733471, compound
https://huagongshe.com/reaction/2278810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | p-Nitro-D-phenylalanine | HCID 679497 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | Methyl 4-nitro-L-phenylalaninate hydrochloride | HCID 11715866 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131733471 | HCID 131733471 | — |
Reaction Steps
2.0 g (5.39 mmol) Chas-D-Phe(4-NO2)—OH and 1.42 g (5.39 mmol) H-Phe(4-NO2)—OMe.HCl were suspended in 30 ml of DMF and 2.82 g (5.39 mmol) of PyBOP and 2.81 ml (16.16 mmol) of DIPEA was added at 0° C. After 2 h of stirring at 0° C., the solvent was removed in vacuo and the brown residue resuspended in 5% KHSO4 soln./EtOAc. The organic phase was washed 3× with 5%-KHSO4 soln., 1× with sat. NaCl soln., 3× with sat. NaHCO3-soln., and 3× with sat. NaCl soln., subsequently dried with MgSO4, filtered, and the solvent was removed in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133194B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-cdea035f35e24810b413ee4f7f8241a2 |
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| Source note | uspto-grants-2015_09 |
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