HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281184Generated: November 1, 2026
Diisopropylethylamine → HCID 11082969, compound
https://huagongshe.com/reaction/1281184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(2-Oxo-1(2H)-pyridyl)-N,N,N',N'-tetramethyluronium Tetrafluoroborate | HCID 2733204 | — |
| Reactant | (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid | HCID 10942966 | — |
| Reactant | HCID 23382091 | HCID 23382091 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11082969 | HCID 11082969 | — |
Reaction Steps
In analogy with Example 2, 0.42 ml of Hünig's base is added to 0.193 g (1.1 mmol) of N-methoxycarbonyl-(L)-valine and 0.327 g (1.1 mmol) of TPTU in 3 ml of DMF and the whole is stirred at RT for 10 min. After that, 0.63 g (1 mmol) of 1-[p-(N,N-diethylamino)-phenyl]-4(S)-hydroxy-2-amino-5(S)-[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane hydrochloride (Example 2f), dissolved in 2 ml of DMF, is added and the mixture is stirred at RT for 21 h. After working-up in the same way as described for Example 2, the residue is digested in DIPE and the title compound is filtered off. The suction filter residue is washed once again with DIPE and dried in a heated desiccator at 45° C. TLC: Rf0.50 (ethyl acetate). HPLC20-100: tret=10.93; FAB MS (M+H)+=685.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451973B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-f90c7e762bdb4dcbba289b8d9aba3394 |
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| Source note | uspto-grants-2002_09 |
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