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HRID 562309作成日:2026年10月27日

Prolinol, (R)- → 5-(5-{[(2R)-2-(hydroxymethyl)-1-pyrrolidinyl]methyl}-3-thienyl)-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamide

https://huagongshe.com/reaction/562309

反応式

関与物質

役割名称HCID仕込み量
反応物Prolinol, (R)-HCID 2724541—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物5-(5-formyl-3-thienyl)-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamideHCID 57732783—
触媒Acetic AcidHCID 176—
溶媒Dimethyl SulfoxideHCID 679—
生成物5-(5-{[(2R)-2-(hydroxymethyl)-1-pyrrolidinyl]methyl}-3-thienyl)-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamideHCID 5773266669.7%

反応手順

To a solution of 5-(5-formyl-3-thienyl)-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamide (25 mg, 0.054 mmol) in DMSO (2 mL) was added (2R)-2-pyrrolidinylmethanol (101.15 mg, 1 mmol) and 2 drops of acetic acid. The resulting mixture was stirred at room temperature for 4 h followed by an addition of sodium triacetoxyborohydride (212 mg, 0.54 mmol). The mixture was reacted overnight. It was then purified by Gilson Preparatory HPLC to give 20.5 mg of the title compound (69.7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063071B2
出典データセットuspto-grants-2011_11
ORD IDord-8aaf73d593a14a5992092a67a51cf495
出典メモuspto-grants-2011_11