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HRID 2177126作成日:2026年10月27日

Cesium carbonate → [7-(2-Benzyloxycarbonylamino-ethyl)-1-(3-chloro-benzyl)-1,2,3,4-tetrahydro-naphthalen-2-yl]-carbamic acid ethyl ester

https://huagongshe.com/reaction/2177126

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Potassium benzyl N-[2-(trifluoroboranuidyl)ethyl]carbamateHCID 49761741—
反応物8-(3-Chlorobenzyl)-7-(ethoxycarbonylamino)-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonateHCID 57476723—
触媒palladium(II) acetateHCID 167845—
溶媒Toluene waterHCID 22272177—
生成物[7-(2-Benzyloxycarbonylamino-ethyl)-1-(3-chloro-benzyl)-1,2,3,4-tetrahydro-naphthalen-2-yl]-carbamic acid ethyl esterHCID 5747672275.6%

反応手順

A mixture of potassium (2-(benzyloxycarbonylamino)ethyl)trifluoroborate (1,130 g, 3.96 mmol), cesium carbonate (2.58 g, 7.93 mmol), 8-(3-chlorobenzyl)-7-(ethoxycarbonylamino)-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonate (1.3 g, 2.64 mmol), Pd(OAc)2 (0.030 g, 0.132 mmol) and 2-dicyclohexyphosphino-2′,6′-di-1-propoxy-1,1′-biphenyl (0.130 g, 0.264 mmol) under N2 in toluene/water 3:1 (15 ml) was heated to refluxed for 13 h. The reaction was filtered, the solvent evaporated and the residue purified by chromatography to afford 1.04 g of product as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09067871B2
出典データセットuspto-grants-2015_06
ORD IDord-9f7119622a304926acf87d150dfec4bb
出典メモuspto-grants-2015_06