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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1750461Erstellt: 25. Oktober 2026

Hydrochloric Acid → HCID 118308082, Verbindung

https://huagongshe.com/reaction/1750461

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
Edukt1,4-DioxaneHCID 31275—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt(1S,2S)-trans-N-Boc-1,2-cyclopentanediamineHCID 17040218—
Edukt2-(3-Methyl-1,2,4-oxadiazol-5-yl)benzoic acidHCID 23146305—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 118308082HCID 118308082—

Reaktionsschritte

A mixture of 2-(3-methyl-1,2,4-oxadiazol-5-yl)benzoic acid (CAS number 475105-77-2; 0.84 g, 4.12 mmol), tert-butyl N-[(1S,2S)-2-aminocyclopentyl]carbamate (CAS number 586961-34-4; 0.75 g, 3.74 mmol), HATU (2.14 g, 5.62 mmol) and triethylamine (1.57 ml, 11.23 mmol) was stirred in dry DMF (12.5 ml) at room temperature for 17 hours. The reaction mixture was partitioned between ethyl acetate and water, washed with water and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The crude material was then purified by column chromatography (silica, 0-100% ethyl acetate/petrol). The resulting cream solid was recrystalised from ethyl acetate, to which was then added methanol (10 ml) and HCl in 1,4-dioxane (4M, 4.68 ml, 18.72 mmol) and the reaction was stirred at room temperature for 17 hours. The reaction was concentrated in vacuo and azeotropically distilled with toluene to afford the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09156829B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-6e020f263d164325bcfa26555829af99
Quellennotizuspto-grants-2015_10