反应 #452475

ord-83cf8d208096407f9854c5332bf0ae09

反应方程式

O
water
Clc1nccc2ccccc12
1-chloroisoquinoline
c1ccc(CN2CCNCC2)cc1
1-benzylpiperazine
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
c1ccc(CN2CCN(c3nccc4ccccc34)CC2)cc1
product
收率 40.6%
c1ccc(CN2CCN(c3nccc4ccccc34)CC2)cc1
1-[4-Benzyl-(1-piperazinyl)]isoquinoline
收率 40.6%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The yellow solution was heated at 110° C. for 7 h
  2. 2
    萃取extracted with ether (2×50 ml)
  3. 3
    干燥The extracts were dried (Na2SO4)
  4. 4
    浓缩concentrated in vacuo
  5. 5
    其他The residue was chromatographed (SiO2 ; ethyl acetate)

实验过程

A solution of 1-chloroisoquinoline (1.64 g 10 mmol) in dry DMF (5 ml) was added to a stirred solution of 1-benzylpiperazine (1.85 g, 10.5 mmol) and N,N-diisopropylethylamine (2 ml, 1.5 g, 11.5 mmol) in dry DMF (5 ml) under Ar at room temperature. The solution was stirred at room temperature for 17 h. The yellow solution was heated at 110° C. for 7 h, treated with water (100 ml) and extracted with ether (2×50 ml). The extracts were dried (Na2SO4) and concentrated in vacuo. The residue was chromatographed (SiO2 ; ethyl acetate) to give the product (1.233 g).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06127357uspto-grants-2000_10