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HRID 2272028作成日:2026年10月25日

3-Bromopyridine-2-carboxylic Acid → cis-6-Methoxy-5-methyl-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine

https://huagongshe.com/reaction/2272028

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromopyridine-2-carboxylic AcidHCID 2050129—
反応物2-(3-Methoxy-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 20580667—
生成物cis-6-Methoxy-5-methyl-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridineHCID 67222612—

反応手順

The title compound is prepared from 3-bromo-pyridine-2-carboxylic acid and 2-(3-methoxy-2-methyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (may be prepared as in WO 2001053268 described) following the synthetic sequence and protocols described for Intermediate 41; since 3-bromo-pyridine-2-carboxylic acid instead of 3-bromo-pyridine-2-carbonitrile is used for the Suzuki-Miyaura coupling (Step 1 of Intermediate 41), hydrolysis of the nitrile (Step 2 of Intermediate 41) is omitted.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09120769B2
出典データセットuspto-grants-2015_09
ORD IDord-57a5dc1c4cde4e93a5e5e91367de085e
出典メモuspto-grants-2015_09