Water → 2-Tert-butyl-5-(4-methylpiperazin-1-yl)-6-nitrobenzothiazole

HRID 5789

반응식

HRID 5789 반응식
[C:1]([C:5]([NH:7][C:8]1[CH:13]=[C:12](Cl)[C:11]([N+:15]([O-:17])=[O:16])=[CH:10][C:9]=1Cl)=[S:6])([CH3:4])([CH3:3])[CH3:2].[CH3:19][N:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1.O>CS(C)=O>[C:1]([C:5]1[S:6][C:9]2[CH:10]=[C:11]([N+:15]([O-:17])=[O:16])[C:12]([N:23]3[CH2:24][CH2:25][N:20]([CH3:19])[CH2:21][CH2:22]3)=[CH:13][C:8]=2[N:7]=1)([CH3:4])([CH3:3])[CH3:2]

참가 물질

5

반응물 3

HCID 962WaterHCID 531671-MethylpiperazineHCID 54175336N-t-butylthiocarbonyl-2,5-dichloro-4-nitroaniline

생성물 1

HCID 197942002-Tert-butyl-5-(4-methylpiperazin-1-yl)-6-nitrobenzothiazole

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

A solution of 171 g of N-tert-butylthiocarbonyl-2,5-dichloro-4-nitroaniline (described in European patent application No. 85810418.5 published under No. 0175650) and 605 ml of N-methylpiperazine in 1700 ml of dimethylsulphoxide is heated at 140° for 8 hours, cooled and poured into water. The solid is filtered, washed with water and cold isopropanol to yield 2-tert-butyl-5-(4-methylpiperazin-1-yl)-6-nitrobenzothiazole, melting at 132°-135°.

후처리

  1. temperaturecooled
  2. filtrationThe solid is filtered
  3. washwashed with water and cold isopropanol

출처 및 근거

ORD 기록
ord-8d6c5e55a6af4dfdb2e2e90fcdc60967
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05246927

연결된 노트

불러오는 중…