反应 #1246

ord-48ed68423d4a4e7fb6e576167938191c

反应方程式

c1ccncc1
pyridine
CC(C)(C)[Si](C)(C)Cl
TBDMSCl
N[C@H](CO)Cc1c[nH]cn1
histidinol
[H-].[Na+]
NaH
Cl.Cl.N[C@H](CO)Cc1c[nH]cn1
histidinol dihydrochloride
ClCCl.N
NH3 CH2Cl2
N[C@H](CO)Cc1c[nH]cn1
14
N[C@H](CO)Cc1c[nH]cn1
histidinol

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他resulting in moderate gas evolution
  2. 2
    workup.STIRRINGThe solution was stirred for 1.5 h
  3. 3
    浓缩concentrated in vacuo and flash
  4. 4
    其他chromatographed on silica with 15% CH3OH

实验过程

TBDMS protected histidinol 14--To a stirred solution of 205 mg (5.1 mmol) of NaH washed 3× with hexane, under argon, in 3.0 mL DMF was added in portions 500 mg (2.3 mmol) of histidinol dihydrochloride, resulting in moderate gas evolution. The solution was stirred for 1.5 h, then 1.8 mL (23 mmol) of anhydrous pyridine and 693.0 mg (4.6 mmol) of TBDMSCl was added. The solution was stirred for 1.5 h, concentrated in vacuo and flash chromatographed on silica with 15% CH3OH.NH3 /CH2Cl2 to yield 14.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723592uspto-grants-1998_03