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HRID 266278作成日:2026年10月27日

p-Bromobenzenesulfonyl chloride → (RS)-2-(4-bromobenzenesulfonyl-amino)-N-(4-(ethoxycarbonylmethyl) phenyl)-3-(tetrahydro-pyran-2-yloxy)propanamide

https://huagongshe.com/reaction/266278

反応式

関与物質

役割名称HCID仕込み量
反応物p-Bromobenzenesulfonyl chlorideHCID 7396—
反応物(RS)-2-(benzyloxycarbonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-3-(tetrahydropyran-2-yloxy)propanamideHCID 19032873—
触媒PalladiumHCID 23938—
生成物(RS)-2-(4-bromobenzenesulfonyl-amino)-N-(4-(ethoxycarbonylmethyl) phenyl)-3-(tetrahydro-pyran-2-yloxy)propanamideHCID 1903291367.2%

反応手順

The procedure described in Example 15 was repeated, except that (RS)-2-(benzyloxycarbonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-3-(tetrahydropyran-2-yloxy)propanamide (2.0 g) was hydrogenolyzed in the presence of 10% Pd-C, and then, reacted with 4-bromobenzenesulfonyl chloride (2.08 g) to obtain (RS)-2-(4-bromobenzenesulfonyl-amino)-N-(4-(ethoxycarbonylmethyl) phenyl)-3-(tetrahydro-pyran-2-yloxy)propanamide (1.58 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05650428
出典データセットuspto-grants-1997_07
ORD IDord-25bab72b70e24bc28a5261471c5ba4fe
出典メモuspto-grants-1997_07