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HRID 651673作成日:2026年10月26日

5'-Chloro-2,2'-bithiophene-5-sulfonyl chloride → 2-[3-(S)-(5'-Chloro-[2,2']bithiophenyl-5-sulfonylamino)-2-oxo-pyrrolidin-1-ylmethyl]pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/651673

反応式

関与物質

役割名称HCID仕込み量
反応物5'-Chloro-2,2'-bithiophene-5-sulfonyl chlorideHCID 22017280—
反応物2-[3-(S)-Amino-2-oxo-pyrrolidin-1-ylmethyl)-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl esterHCID 54368269—
生成物2-[3-(S)-(5'-Chloro-[2,2']bithiophenyl-5-sulfonylamino)-2-oxo-pyrrolidin-1-ylmethyl]pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl esterHCID 69709209—

反応手順

The title compound is prepared as described in EXAMPLE 56, Part A using 5′-chloro-[2,2′]bithiophenyl-5-sulfonyl chloride and 2-[3-(S)-amino-2-oxo-pyrrolidin-1-ylmethyl)-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester as starting material. The crude product can be purified by column chromatography eluting with 5% MeOH/CH2Cl2 to give the title compound as a white solid or used in the subsequent step after an aqueous work-up without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06281227B1
出典データセットuspto-grants-2001_08
ORD IDord-45cbc60524734fecb891f6b069bdafe8
出典メモuspto-grants-2001_08