반응 #5889

ord-0021d0cc1d434e90be2099cbc1a36c49

반응 방정식

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
수율 69.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with water
  2. 2
    건조dried over anhydrous sodium sulphate
  3. 3
    기타evaporated
  4. 4
    기타to get a sticky residue which
  5. 5
    기타is triturated with isopropanol
  6. 6
    여과filtered

실험 절차

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°.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05246927uspto-grants-1993_09