反应 #1914877

ord-98947d6412c24e39ba9cbc432f32cb30

反应方程式

[H-].[Na+]
NaH
CC(C)(C)C(=O)Nc1nc(NC(=O)C(C)(C)C)c2c(CBr)c(Br)sc2n1
2,4-bis(pivaloylamino)-5-bromomethyl-6-bromothieno[2,3-d]pyrimidine
c1ccc(Nc2ccccc2)cc1
diphenylamine
[H-].[Na+]
NaH
CO
MeOH
Brc1cc2cncnc2s1
6-bromothieno[2,3-d]pyrimidine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the solvent is evaporated
  2. 2
    其他the residue is chromatographed on silica gel

实验过程

A mixture of 2,4-bis(pivaloylamino)-5-bromomethyl-6-bromothieno[2,3-d]pyrimidine prepared in Step 2 above (200 mg, 0.4 mmol), diphenylamine (1.3 g, 0.77 mmol) and NaH (50 mg, 2.1 mmol) in dry THF (10 mL) is stirred at room temperature for 2 days, the excess NaH is decomposed with MeOH (1 mL), the solvent is evaporated, and the residue is chromatographed on silica gel to obtain 2,4-bis(pivaloylamino)-5-N,N-diphenylaminomethyl)-6-bromothieno[2,3-d]pyrimidine.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07056911B1uspto-grants-2006_06