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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245217Generated: October 25, 2026

Hydrochloric Acid → Ac-D-Lys(Z)-D-Pro-D-Val-NH2

https://huagongshe.com/reaction/2245217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
Reactant(R)-2-amino-3-methylbutanamideHCID 444079—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantAc-D-Lys(Z)-D-Pro-OHHCID 131727990—
SolventDimethylformamideHCID 6228—
ProductAc-D-Lys(Z)-D-Pro-D-Val-NH2HCID 131727991—

Reaction Conditions

Temperature5 °C

Reaction Steps

In an inert thermostable reactor provided with a mechanical stirrer, 94.25 g of Ac-D-Lys(Z)-D-Pro-OH (XI) (224.7 mmol) are introduced followed by 470 ml of DMF. 32.58 g of HCl. H-D-Val-NH2 (V) (213.5 mmol, 0.95 eq) and 85.22 g of HBTU (1 eq) are then added. The medium is cooled down to 5° C., and 96.6 ml of ethyldiisopropylamine (2.5 eq) are added dropwise within 15 minutes. This is allowed to reach 0° C. again and after 1.30 to 2 hours, a strong crystallization could be observed. The reaction completion is CCM controlled. The reaction medium is then poured onto 2350 ml of AcOEt, stirred for 15 minutes, filtered and washed successively with 470 ml of AcOEt and 470 ml of diisopropyl ether. The derivate (XII) is vacuum dried at 25° C. This way, 107.2 g (92%) pf Ac-D-Lys(Z)-D-Pro-D-Val-NH2 are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683026B2
Source datasetuspto-grants-2010_03
ORD IDord-4ba63546249646fb9ba69a24b15dfec2
Source noteuspto-grants-2010_03