반응 #2254154

ord-8cd3830461cc476896c7180c97132376

반응 방정식

CC(C)[S+](N)C(C)C.Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1
S,S-Diisopropyl-S-aminosulfonium 2,4,6-trimethyl-phenylsulfonate
O=c1[nH]c2c(Cl)cc(Cl)cc2c(=O)o1
6,8-dichloro-1H-benzo[d][1,3]oxazine-2,4-dione
O
Water
CC(C)(C)[O-].[K+]
potassium tert-butanolate
CC(C)S(=NC(=O)c1cc(Cl)cc(Cl)c1N)C(C)C
title compound
CC(C)S(=NC(=O)c1cc(Cl)cc(Cl)c1N)C(C)C
2-amino-N-(bis-2-propyl-λ4-sulfanylidene)-3,5-dichloro-benzamide

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to come to room temperature
  2. 2
    기타the organic phase was separated
  3. 3
    추출the aqueous phase further extracted with methylene chloride (2×100 mL)
  4. 4
    건조The combined organic extracts were dried (MgSO4)
  5. 5
    농축concentrated in vacuo

실험 절차

To a suspension of 6,8-dichloro-1H-benzo[d][1,3]oxazine-2,4-dione (45.0 g, 70.7 mmol) in methylene chloride (500 mL) was added S,S-Diisopropyl-S-aminosulfonium 2,4,6-trimethyl-phenylsulfonate (77.6 g, 234 mmol). The reaction mixture was cooled to 0° C. and potassium tert-butanolate (8.73 g, 77.8 mmol) was added after which the reaction was allowed to come to room temperature and stirred for 16 h. Water (200 mL) and methylene chloride (50 mL) were then added, the organic phase was separated and the aqueous phase further extracted with methylene chloride (2×100 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo to afford the title compound (62.8 g, quant.).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09044016B2uspto-grants-2015_06