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HRID 73208作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Dibutyltin dichlorideHCID 12688—
反応物PhenylsilaneHCID 12752—
反応物Methyl 3-amino-2-thiophenecarboxylateHCID 89652—
反応物Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
溶媒TetrahydrofuranHCID 8028—
生成物4-(2-Methoxycarbonyl-thiophen-3-ylamino)-piperidine-1-carboxylic acid benzyl esterHCID 68424861101.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829030B2
出典データセットuspto-grants-2014_09
ORD IDord-7cbc4f34d00440aabc26ce241c80932d
出典メモuspto-grants-2014_09