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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281184Generated: November 1, 2026

Diisopropylethylamine → HCID 11082969, compound

https://huagongshe.com/reaction/1281184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(2-Oxo-1(2H)-pyridyl)-N,N,N',N'-tetramethyluronium TetrafluoroborateHCID 2733204—
Reactant(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acidHCID 10942966—
ReactantHCID 23382091HCID 23382091—
SolventDimethylformamideHCID 6228—
ProductHCID 11082969HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451973B1
Source datasetuspto-grants-2002_09
ORD IDord-f90c7e762bdb4dcbba289b8d9aba3394
Source noteuspto-grants-2002_09