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HRID 73208Erstellt: 23. Oktober 2026

Dibutyltin dichloride → 4-(2-Methoxycarbonyl-thiophen-3-ylamino)-piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/de/reaction/73208

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibutyltin dichlorideHCID 12688—
EduktPhenylsilaneHCID 12752—
EduktMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
EduktBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(2-Methoxycarbonyl-thiophen-3-ylamino)-piperidine-1-carboxylic acid benzyl esterHCID 68424861101,4%

Reaktionsschritte

Reductive amination of 3-amino-thiophene-2-carboxylic acid methyl ester (3.0 g, 19.1 mmol) and 4-oxo-piperidine-1-carboxylic acid benzyl ester (4.46 g, 19.1 mmol) in THF (4.6 mL) employing Bu2SnCl2 (0.598 g, 1.92 mmol) and PhSiH3 (2.58 mL, 21.6 mmol) was carried out as described for example 19, step 1 gave 4-(2-methoxycarbonyl-thiophen-3-ylamino)-piperidine-1-carboxylic acid benzyl ester (7.25 g, quantitative). NMR 1H (CDCl3, 400 MHz): 7.4-7.3 (m, 6H), 6.9-6.78 (m, 1H), 6.7-6.6 (m, 1H), 5.14 (s, 2H), 4.15-4.0 (m, 2H), 3.81 (s, 3H), 3.6-3.45 (m), 3.1 (brt, 2H), 2.1-1.9 (m, 2H), 1.6-1.45 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829030B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-7cbc4f34d00440aabc26ce241c80932d
Quellennotizuspto-grants-2014_09