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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 899397Erstellt: 24. Oktober 2026

Ammonia → Butanedioic acid, 1,4-di-2-propen-1-yl ester

https://huagongshe.com/de/reaction/899397

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktDiisopropylethylamineHCID 81531—
EduktSuccinateHCID 160419—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
LösungsmittelDimethylformamideHCID 6228—
ProduktButanedioic acid, 1,4-di-2-propen-1-yl esterHCID 70215—

Reaktionsschritte

11 (240 mg, 0.46 mmol) and HATU (350 mg, 0.92 mmol) were dissolved in DMF (2 mL) and diisopropylethylamine (0.16 mL, 0.92 mmol) was added. The mixture was stirred for 15 min at ambient temperature, and then treated with anhydrous ammonia for 20 min. Stirring was continued overnight. DMF was removed in vacuo, and the residue was diluted with ethyl acetate, washed with water and brine, then dried over MgSO4. After evaporation of the solvent, the residue was purified on silica gel (5% methanol/methylene chloride) to afford product 12 as a white solid. 12, a mixture of two diastereomers, was then separated on silica gel, using increasing gradient of 20-50% ethyl acetate-methylene chloride, to give first eluting isomer 12a (43 mg, 18%.) and the second eluting isomer 12b (61 mg, 25%) both as a white solids. 12a: MS m/z 521.2 (MH+). 12b: MS m/z 521.2 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07354914B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-514946d847124c1d9cce44551cd2a668
Quellennotizuspto-grants-2008_04