反应 #218057

ord-6e084373031c430aadbf579b3ebd9e30

反应方程式

NC(=O)c1cnc(Oc2ccc(C=O)cc2)cn1
5-(4-formylphenoxy)pyrazine-2-carboxamide
CC(C)CCN
3-methylbutylamine
[BH4-].[Na+]
NaBH4
CC(C)CCNCc1ccc(Oc2cnc(C(N)=O)cn2)cc1
title compound
收率 31.2%
CC(C)CCNCc1ccc(Oc2cnc(C(N)=O)cn2)cc1
5-{4-[(3-Methylbutylamino)methyl]phenoxy}pyrazine-2-carboxamide
收率 31.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Dry the column in a vacuum oven at room temperature
  2. 2
    其他Purify
  3. 3
    洗涤by eluting through a 10 g ISCO® column with 2.0 M NH3 in methanol, ethyl acetate and hexanes

实验过程

Place 5-(4-formylphenoxy)pyrazine-2-carboxamide (0.150 g, 0.617 mmol), 3-methylbutylamine (0.0537 g, 0.617 mmol) and 3 Å molecular sieves in a vial. Add methanol (3.1 mL), cap and stir overnight. Add NaBH4 (in excess over two portions) and stir until the gasses stop evolving. Load the reaction mixture directly onto a 5 g ISCO® pre-load column. Dry the column in a vacuum oven at room temperature. Purify by eluting through a 10 g ISCO® column with 2.0 M NH3 in methanol, ethyl acetate and hexanes to give the title compound (0.0606 g, 31.2%): MS ES+ 315.1 (M+H)+, base peak 228.0 (M−C5H12N)+; HPLC [YMC-Pack Pro C-18 (150×4.6 mm, S-5 microm), 0.1% TFA/acetonitrile in 0.1% TFA/water at 1.0 mL/min, 5-95% over 19 min], tR=8.5 min., 96.4% purity.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07381719B2uspto-grants-2008_06