Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535166Generated: October 26, 2026

Hydrochloric Acid → HCID 178471713, compound

https://huagongshe.com/reaction/535166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Carboxy-1,2,3-triazoleHCID 140120—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(2S,4R)-5-Biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-2-methyl-pentanoic acidHCID 68181022—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178471713HCID 178471713—

Reaction Steps

1,2,3-Triazole-4-carboxylic acid (11.5 mg, 102 μmol, 1.2 eq.) and HATU (38.6 mg, 102 μmol, 1.2 eq.) were dissolved in DMF (0.9 mL) and stirred at room temperature for 5 minutes. DIPEA (29.5 μL, 2.0 eq.) was added to yield the activated acid. (2S,4R)-5-Biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-2-methyl-pentanoic acid (35 mg, 85 μmol, 1.0 eq.) was dissolved in EtOH and 4 M of HCl in dioxane (423 μL) was added. The mixture was heated to 60° C. overnight, then concentrated to dryness and purified by reverse phase chromatography (5-60% MeCN in water over 18 minutes. The clean fractions were combined and dried under vacuum to dryness, then combined with the activated acid. After 20 minutes, the reaction was quenched with water and the product was dried under vacuum and purified by preparative HPLC to yield the title compound (4 mg, >95% purity. MS m/z [M+H]+ calc'd for C24H28N4O4, 437.21. found 437.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853427B2
Source datasetuspto-grants-2014_10
ORD IDord-e0c57e16cd614bc5ac56c2366bdf9f93
Source noteuspto-grants-2014_10