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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281185Generated: October 31, 2026

Diisopropylethylamine → HCID 23382096, compound

https://huagongshe.com/reaction/1281185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(2-Oxo-1(2H)-pyridyl)-N,N,N',N'-tetramethyluronium TetrafluoroborateHCID 2733204—
ReactantHCID 10647477HCID 10647477—
Reactant(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acidHCID 10942966—
SolventDimethylformamideHCID 6228—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 23382096HCID 23382096—

Reaction Steps

In analogy with Example 2e, 1.5 ml of Hünig's base are added to 0.77 g (4.3 mmol) of N-methoxycarbonyl-(L)-valine and 1.3 g (4.3 mmol) of TPTU in 20 ml of DMF and the whole is stirred at RT for 5 min. After that, 2.0 g (4.3 mmol) of 1-[p-(N,N-diethylamino)phenyl]-4(S)-hydroxy-2-(tert-butyloxycarbonyl)amino-5(S)-amino-6-phenyl-2-azahexane (Example 2d), dissolved in DMF, are added and the mixture is stirred at RT for 2 h. After working up in the same manner as described for Example 2e, 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 60° C., with the title compound thereby being obtained. TLC: Rf=0.80 (methylene chloride/methanol). HPLC20-100: tret=11.79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451973B1
Source datasetuspto-grants-2002_09
ORD IDord-d3add5a18b2d46eda252ec26a5fc2d2c
Source noteuspto-grants-2002_09