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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63673Erstellt: 24. Oktober 2026

Diisopropylethylamine → HCID 73331267, Verbindung

https://huagongshe.com/de/reaction/63673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4,4-DifluoroprolineHCID 15216102—
Edukt6-Bromomethyl-4-(2-chloro-4-fluoro-phenyl)-2-thiazol-2-yl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl esterHCID 89995963—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 73331267HCID 73331267—

Reaktionsschritte

To a stirred solution of 6-bromomethyl-4-(2-chloro-4-fluoro-phenyl)-2-thiazol-2-yl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl ester (0.049 g, 0.11 mmol) and (S)-4,4-difluoro-pyrrolidine-2-carboxylic acid (0.044 g, 0.17 mmol) in 1,2-dichloroethane (5 mL) was added dropwise DIPEA (0.078 mL, 0.45 mmol). The reaction mixture was stirred at room temperature until the disappearance of starting material which was checked by LC/MS. The mixture was diluted with EtOAc (50 mL) and washed successively with saturated aqueous NH4Cl solution and brine. The organic layer was separated and dried over Na2SO4. The solvent was concentrated in vacuo and the crude product was purified by prep-HPLC to give 6-((S)-2-carboxy-4,4-difluoro-pyrrolidin-1-ylmethyl)-4-(2-chloro-4-fluoro-phenyl)-2-thiazol-2-yl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl ester (Example 1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447086B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-b58e6cfc871c421eb871900673d052a7
Quellennotizuspto-grants-2016_09