反应 #543559

ord-4f38dba369d24a57800074358c31c7c7

反应方程式

O=[As]c1ccc(NC(=O)CSCCC(=O)N[C@@H](CC(=O)O)C(=O)O)cc1
N-(3-(4-arsenosophenylcarbamoylmethylthio)propanoyl)-L-aspartic acid
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
O=C([O-])CC[C@H](NC(=O)CCS)C(=O)[O-].[Na+].[Na+]
disodium N-(3-mercaptopropanoyl)-L-glutamate
O=C([O-])O
bicarbonate
O=[As]c1ccc(NC(=O)CSCCC(=O)N[C@@H](CCC(=O)O)C(=O)O)cc1
N-(3-(4-arsenosophenylcarbamoylmethylthio)propanoyl)-L-glutamic acid

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他before leaving overnight
  2. 2
    浓缩The active concentration of trivalent arsenic

实验过程

The procedure used was the same as for N-(3-(4-arsenosophenylcarbamoylmethylthio)propanoyl)-L-aspartic acid, using 2.63 mL (184 μmol) of 70.0 mM BRAO in DMSO, the disulfide of disodium N-(3-mercaptopropanoyl)-L-glutamate (0.61 g), 0.5 M bicarbonate buffer, pH 9 (10.52 mL, 5.3 mmol), and 0.69 M triphenylphosphine in DMSO (1.7 mL, 1.2 mmol). In this case, DMSO (2 mL) was added to the precipitated mixture before leaving overnight. The active concentration of trivalent arsenic was found to be 15.4 mM (10.3 mL of solution).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186695B2uspto-grants-2007_03