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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1804645Erstellt: 25. Oktober 2026

1,2-Dichloroethane → Tert-butyl (2R,5S)-2-[(R)-hydroxy(phenyl)methyl]-5-(4-{[5-(1H-pyrazol-1-yl)piperidin-1-yl]carbonyl}benzyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1804645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktDiisopropylethylamineHCID 81531—
EduktHOAtHCID 181649—
Edukt4-(1H-Pyrazol-1-yl)piperidineHCID 21193045—
Edukt4-({(2S,5R)-1-(tert-butoxycarbonyl)-5-[(R)-hydroxy(phenyl)methyl]pyrrolidin-2-yl}methyl)benzoic acidHCID 67058707—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl (2R,5S)-2-[(R)-hydroxy(phenyl)methyl]-5-(4-{[5-(1H-pyrazol-1-yl)piperidin-1-yl]carbonyl}benzyl)pyrrolidine-1-carboxylateHCID 8666675481%

Reaktionsschritte

To a solution of 4-{((2S,5R)-1-(tert-butoxycarbonyl)-5-[(R)-hydroxy(phenyl)methyl]pyrrolidin-2-yl)methyl}benzoic acid (82 mg, 0.2 mmol) and 4-(1H-pyrazol-1-yl)piperidine (30 mg, 0.2 mmol) in 1.5 mL anhydrous DMF was added a 0.5 M solution of HOAt in DMF (0.4 mL, 0.2 mmol) followed by EDC (78 mg, 0.4 mmol) and DIEA (70 μL, 0.4 mmol). The resulting mixture was stirred at RT under nitrogen atmosphere for 16 h. The mixture was washed with water and extracted with dichloromethane (2×5 mL). The organics were combined, dried over sodium sulfate, filtered and concentrated in vacuum. The residue was purified by preparative TLC plate (1000 uM) eluting with 5% MeOH in dichloromethane to afford the title compound (88 mg, 81%). ESI-MS calculated for C32H40N4O4: Exact Mass: 544.30. Found 545.30 (MH)4 and 567.28 (MNa)+,

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08354403B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-7c0b9da5d7e54e52b1548a49c1349770
Quellennotizuspto-grants-2013_01