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HRID 131656Erstellt: 26. Oktober 2026

3-Heptanone → 2-(s)-(1-Propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide

https://huagongshe.com/reaction/131656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-HeptanoneHCID 7802—
EduktSodium SulfateHCID 24436—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl saltHCID 131726918—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt2-(s)-(1-Propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amideHCID 11654783—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A mixture of 2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl salt (100 mg, 0.265 mmol) and 3-heptanone (0.1 mL), acetic acid (0.2 mL), sodium sulfate and sodium cyanoborohydride (100 mg) in dichloroethane (2 mL) and methanol (1 mL) was stirred at 40° C. overnight. The mixture was quenched with water, basified by dilute sodium hydroxide, and extracted with methylene chloride. The organic layer was concentrated to dryness. The residue was purified by Biotage silica gel column chromatography to isolate 2-(S)-(1-propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide as a colorless oil, LC-MS, RT=2.2 min, M+1=426.5.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384968B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-59679df6d87c47658f1cf87b4a0d71bc
Quellennotizuspto-grants-2008_06