反应 #1543039

ord-ac52f0db751c454eab937e669a073c1b

反应方程式

[Na+].[OH-]
NaOH
N[C@@H](Cc1cc(I)c(Oc2cc(I)c(O)c(I)c2)c(I)c1)C(=O)O
L-thyroxine
[Na+].[OH-]
NaOH
Cl
HCl
O=C(CI)ON1C(=O)CCC1=O
iodoacetic acid N-hydroxysuccinimide ester
CC(=O)NI.N[C@@H](Cc1cc(I)c(Oc2cc(I)c(O)c(I)c2)c(I)c1)C(=O)O
Thyroxine N-iodoacetamide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他reaction
  2. 2
    其他The precipitate was collected by centrifugation
  3. 3
    洗涤washed with 1 ml of methanol and 4 mls of water
  4. 4
    干燥After centrifugation the pellet was dried under vacuum to 82 mg of an off-white solid

实验过程

78 mg (0.1 mmole) of L-thyroxine was dissolved in 1.0 ml of methanol on addition of 34 mls (0.2 mmole) of 6N NaOH and sonication in a bath sonicator. 48 mg of iodoacetic acid N-hydroxysuccinimide ester was added and the mixture vortexed. 8.5 mls of 6N NaOH was added and the mixture vortexed. TLC (chloroform:methanol:acetic acid 50:6:2 on silica gel) indicated complete reaction. 50 mls of 6N HCl was added and then 4 mls of water and formed a precipitate. The precipitate was collected by centrifugation and washed with 1 ml of methanol and 4 mls of water. After centrifugation the pellet was dried under vacuum to 82 mg of an off-white solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05843634uspto-grants-1998_12