反応 #1352210

反応方程式

2-methyl-4,5-(methylenedioxy)benzaldehyde

N-(4-chloro-5-methyl-3-isoxazolyl)-N-(methoxyethoxymethyl)thieno [2,3-b]pyridine-3-sulfonamide

t-BuLi

→

title compound

収率 36.0%

N-(4-chloro-5-methyl-3-isoxazolyl)-N-(methoxyethoxymethyl)-2 -[α-hydroxy-2-methyl-4,5-(methylenedioxy)-benzyl]thieno[2,3-b]pyridine-3-sulfonamide

収率 36.0%

溶媒

THF

反応条件

後処理

1. 1
   その他The title compound was prepared by the method of Example 4(B)

実験手順

The title compound was prepared by the method of Example 4(B) using N-(4-chloro-5-methyl-3-isoxazolyl)-N-(methoxyethoxymethyl)thieno [2,3-b]pyridine-3-sulfonamide (0.23 g, 0.54 mmoles), THF (5 ml), t-BuLi (1.7 M, 0.41 ml, 0.70 mmoles) and 2-methyl-4,5-(methylenedioxy)benzaldehyde (0.13 g, 0.81 mmoles)[Example 6(A)]. Flash chromatography (40% EtOAc/hexanes) provided 0.11 g (36%) of the title compound as a light orange oil.

出典