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HRID 18073作成日:2026年10月25日

Triethylamine → 2-(Benzooxazol-2-ylaminomethyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/18073

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-ChlorobenzoxazoleHCID 11986—
反応物tert-Butyl 2-(aminomethyl)piperidine-1-carboxylateHCID 2756482—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Benzooxazol-2-ylaminomethyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 66570237110.9%

反応手順

(RS) 2-Aminomethyl-piperidine-1-carboxylic acid tert butyl ester (0.21 g) and 2-chlorobenzoxazole (0.153 g) and triethylamine (0.1 g) were combined in tetrahydrofuran (10 ml) and stirred at room temperature for 4 hours. The mixture was partitioned between ethyl acetate and water, the organic phase dried and solvent removed at reduced pressure to give the title compound (0.36 g) as an oil that solidified on standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741329B2
出典データセットuspto-grants-2010_06
ORD IDord-97882efc0c7c4fa1915436993b0beb93
出典メモuspto-grants-2010_06