反応 #218181

ord-aaef3d6741b241ada1bb8a0f51d41299

反応方程式

[BH4-].[Na+]
NaBH4
NC(=O)c1cnc(Oc2ccc(C=O)cc2F)cn1
5-(2-fluoro-4-formylphenoxy)pyrazine-2-carboxamide
CCCCCCN
hexylamine
CCCCCCNCc1ccc(Oc2cnc(C(N)=O)cn2)c(F)c1
title compound
収率 62.1%
CCCCCCNCc1ccc(Oc2cnc(C(N)=O)cn2)c(F)c1
5-(2-Fluoro-4-hexylaminomethylphenoxy)pyrazine-2-carboxamide
収率 62.1%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Dry the column in a vacuum oven at room temperature
  2. 2
    その他Purify
  3. 3
    洗浄by eluting through a 40 g ISCO® column with 0% to 15% (2.0 M NH3 in methanol) in 80% (ethyl acetate in hexanes)

実験手順

Place 5-(2-fluoro-4-formylphenoxy)pyrazine-2-carboxamide (Example 737, Part E) (0.400 g, 1.53 mmol), hexylamine (0.170 g, 1.68 mmol) and 3 {acute over (Å)} molecular sieves in a vial. Add methanol (7.7 mL), cap and stir overnight. Add NaBH4 (0.058 g, 1.53 mmol) and stir until the gasses stop evolving. Load the reaction mixture directly onto a 25 g ISCO® pre-load column. Dry the column in a vacuum oven at room temperature. Purify by eluting through a 40 g ISCO® column with 0% to 15% (2.0 M NH3 in methanol) in 80% (ethyl acetate in hexanes) to give the title compound (0.329 g, 62%); TOF MS ES+ 347.2 (M+H)+, HRMS calcd for C18H24N4O2F 347.1883 (M+H)+, found 347.1897, time 0.57 min; HPLC [YMC-Pro pack C-18 (150×4.6 mm, S-5 microm), 0.05% TFA/acetonitrile in 0.05% TFA/water at 1.0 mL/min, 10-20% over 5 min, 20-95% over 18], tR=11.4 min, 94.8% purity.

出典

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