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HRID 1425262作成日:2026年10月27日

Cesium carbonate → Methyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-4-fluorobenzoate

https://huagongshe.com/reaction/1425262

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Binap, (A+-)-HCID 634876—
反応物Methyl 3-bromo-4-fluorobenzoateHCID 7018022—
反応物Benzyl cis(+/-)-[3-methoxypiperidin-4-yl]carbamateHCID 86648490—
触媒palladium(II) acetateHCID 167845—
生成物Methyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-4-fluorobenzoateHCID 8664874461.5%

反応手順

The same operation as in Example (42a) was performed using benzyl cis(±)-[3-methoxypiperidin-4-yl]carbamate obtained in Example (160a) (100 mg, 0.38 mmol), methyl 3-bromo-4-fluorobenzoate (264 mg, 1.13 mmol), palladium acetate (25.5 mg, 0.11 mmol), BINAP (141 mg, 0.23 mmol) and cesium carbonate (370 mg, 1.13 mmol), to obtain 97.4 mg of the title compound as a yellow oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08927588B2
出典データセットuspto-grants-2015_01
ORD IDord-ce39f08fe00e4433aea11174ec7b1f40
出典メモuspto-grants-2015_01