Triethylamine → tert-butyl 5-(1-phenyl-1H-tetrazol-5-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate

HRID 75680

Reaktionsgleichung

CCN(CC)CC.[CH2:8]1[CH:12]2[CH2:13][NH:14][CH2:15][CH:11]2[CH2:10][N:9]1[C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17].Cl[C:24]1[N:28]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[N:27]=[N:26][N:25]=1>O1CCOCC1>[C:29]1([N:28]2[C:24]([N:14]3[CH2:13][CH:12]4[CH2:8][N:9]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH2:10][CH:11]4[CH2:15]3)=[N:25][N:26]=[N:27]2)[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1

Komponenten

Reaktionsbedingungen

Temperatur: 115 °C

Versuchsvorschrift

Et3N (5 mL) was added into a solution of tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (1 g) and 5-chloro-1-phenyl-1H-tetrazole (1 g) in dioxane (50 mL). The mixture was heated to 115° C. for 24 hours. The reaction was quenched with water (50 mL). The aqueous layer was extracted with EtOAc (3×50 mL). The combined organic phase was dried over MgSO4 and concentrated to give a residue which was purified by silica gel chromatography to give tert-butyl 5-(1-phenyl-1H-tetrazol-5-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate.

Aufarbeitung

customThe reaction was quenched with water (50 mL)
extractionThe aqueous layer was extracted with EtOAc (3×50 mL)
dry with materialThe combined organic phase was dried over MgSO4
concentrationconcentrated
customto give a residue which
customwas purified by silica gel chromatography

Quellen und Nachweise

ORD-Eintrag: ord-6e979fb885ae435699149ab8f9ee29c1
Quelldatensatz: uspto-grants-2014_09
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08835454B2

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