HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278812Generated: November 3, 2026
Diisopropylethylamine → HCID 14365061, compound
https://huagongshe.com/reaction/2278812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 2755957 | HCID 2755957 | — |
| Reactant | Methyl 4-nitro-L-phenylalaninate hydrochloride | HCID 11715866 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14365061 | HCID 14365061 | — |
Reaction Steps
1.0 g (3.22 mmol) Boc-D-Phe(4-NO2)—OH (Iris Biotech) and 0.84 g (3.22 mmol) H-Phe(4-NO2)—OMe.HCl (Aldrich) were suspended in 25 ml of DMF and stirred on the ice bath. After addition of 1.66 g (3.22 mmol) of PyBOP and 1.67 ml (9.66 mmol) of DIPEA (pH 7-8), the mixture was stirred at 0° C. for 2.5 h. The solvent was removed in vacuo and the yellow oil was taken up 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. The organic phase was 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-2396abf1cc104981b28f95521cc2fe2a |
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| Source note | uspto-grants-2015_09 |
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