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HRID 1363264Erstellt: 25. Oktober 2026

Dimethylamine → methyl 6-[(dimethylamino)methyl]-4H-thieno[3,2-b]pyrrole-5-carboxylate

https://huagongshe.com/reaction/1363264

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktFormaldehydeHCID 712—
EduktSodium HydroxideHCID 14798—
Eduktmethyl 4H-thieno[3,2-b]pyrrole-5-carboxylateHCID 4058811—
LösungsmittelAcetic AcidHCID 176—
Produktmethyl 6-[(dimethylamino)methyl]-4H-thieno[3,2-b]pyrrole-5-carboxylateHCID 5964857570%

Reaktionsschritte

Under N2, to 9 mL of glacial acetic acid were added N,N-dimethylamine (40% aqueous solution) (437 mg, 9.94 mmol), formaldehyde (37% aqueous solution) (283 mg, 9.90 mmol), and methyl 4H-thieno[3,2-b]pyrrole-5-carboxylate (1.8 g, 9.94 mmol). The temperature was kept between 0-5° C. while the components were added. The reaction mixture was heated at reflux for 1 h, and then allowed to stand at rt for 12 h. The mixture was poured onto 30 g of ice, and was brought to pH 10 by careful addition of 10% sodium hydroxide. The temperature was not allowed to exceed 10° C. while the base was added. The gummy substance that precipitated solidified when stored in the refrigerator overnight. The solid was collected and dried in a vacuum. It was recrystallized from petroleum ether (30-60° C.) to yield methyl 6-[(dimethylamino)methyl]-4H-thieno[3,2-b]pyrrole-5-carboxylate (1.65 g, 70%). 1H NMR (400 MHz, CDCl3) δ ppm 2.36 (s, 6H) 3.86 (s, 3H) 3.89 (s, 2H) 6.85 (d, J=5.32 Hz, 1H) 7.28 (d, J=5.32 Hz, 1H) 9.84 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07884124B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-3a3fa57e64cd4d78b6cd4424a86186d1
Quellennotizuspto-grants-2011_02