反応 #5889

ord-0021d0cc1d434e90be2099cbc1a36c49

反応方程式

CC1CCN(c2cc3nc(C(C)(C)C)sc3cc2N=C=S)CC1
2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole
C1CNCCN1
piperazine
CC1CCN(c2cc3nc(C(C)(C)C)sc3cc2NC(=S)N2CCNCC2)CC1
2-tert-butyl-5-(4-methyl-piperidin-1-yl)-6-[(piperazin-1-yl)thiocarbonylamino]benzothiazole
収率 69.6%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄washed with water
  2. 2
    乾燥dried over anhydrous sodium sulphate
  3. 3
    その他evaporated
  4. 4
    その他to get a sticky residue which
  5. 5
    その他is triturated with isopropanol
  6. 6
    ろ過filtered

実験手順

A solution of 3.45 g of 2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole, described in Example 1, and 8.6 g of anhydrous piperazine in 30 ml of chloroform is stirred for 3 hours, washed with water, dried over anhydrous sodium sulphate and evaporated to get a sticky residue which is triturated with isopropanol and filtered to obtain 3 g of 2-tert-butyl-5-(4-methyl-piperidin-1-yl)-6-[(piperazin-1-yl)thiocarbonylamino]benzothiazole, melting at 278°-281°.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05246927uspto-grants-1993_09