反应 #657262

ord-d4bd87fbd14f4d59b5abaf5b8b648ead

反应方程式

CCOC(=O)CN(CCn1nc(COC)cc1COC)CCn1nc(COC)cc1COC
ethyl 2-(bis(2-(3,5-bis(methoxymethyl)-1H-pyrazol-1-yl)ethyl)amino)acetate
[Al+3].[H-].[H-].[H-].[H-].[Li+]
LiAlH4
COCc1cc(COC)n(CCN(CCO)CCn2nc(COC)cc2COC)n1
title compound
收率 60.0%
COCc1cc(COC)n(CCN(CCO)CCn2nc(COC)cc2COC)n1
2-(bis(2-(3,5-bis(methoxymethyl)-1H-pyrazol-1-yl)ethyl)amino)ethanol
收率 60.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他This compound has been obtained

实验过程

This compound has been obtained by reacting a solution of ethyl 2-(bis(2-(3,5-bis(methoxymethyl)-1H-pyrazol-1-yl)ethyl)amino)acetate (280 mg; 0.6 mmol) in dry THF (10 mL) with LiAlH4. The title compound was isolated following the same methodology above described for the synthesis of other (hydroxymethyl)pyrazoles (see example 6). Yield: 60% (170 mg, 0.4 mmol).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09023315B2uspto-grants-2015_05