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HRID 48521作成日:2026年10月23日

Tetramethyltin → 5'-Methylspiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]

https://huagongshe.com/ja/reaction/48521

反応式

関与物質

役割名称HCID仕込み量
反応物TetramethyltinHCID 11661—
反応物Tri-o-tolylphosphineHCID 80271—
反応物Lithium ChlorideHCID 433294—
反応物5'-bromospiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]HCID 10357133—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
溶媒DiglymeHCID 8150—
生成物5'-Methylspiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]HCID 15908242166.3%

反応条件

温度100 °C

反応手順

A solution containing 5′-bromospiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine] (203 mg, 0.687 mmol), tris(dibenzylidineacetone)dipalladium (0) (33 mg, 0.036 mmol), tri(o-tolyl)phosphine (95 mg, 0.312 mmol), lithium chloride (241 mg, 5.69 mmol), and tetramethylstannane (1.0 ml, 1.3 g, 7.2 mmol) in 2-methoxyethyl ether (5 ml) was heated in a bath maintained at 100° C. After 3 h, a further portion of tetramethylstannane (1 ml, 1.3 g, 7.2 mmol) was added, and heating was continued overnight. The solution was filtered, and subjected to purification by HPLC using a gradient of 0-20% 1:1:2 7M methanolic ammonia:methanol:chloroform and chloroform to obtain the title compound (120 mg, 0.519 mmol, 76%) as a pale solid: electrospray MS (m/z, relative intensity) 231 ([MH]+, 100).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703502B2
出典データセットuspto-grants-2004_03
ORD IDord-30448ba81ae5431491787ade7fb36520
出典メモuspto-grants-2004_03