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Thionyl Chloride → N-methane-sulphonyl-3-(2-chloro-5-trifluoromethylphenoxy)benzamide

HRID 649103
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HRID 649103 반응식
NC1C=C(C(F)(F)F)C=C(Cl)C=1OC1C=CC([N+]([O-])=O)=C(C=1)C(OC)=O.S(Cl)(Cl)=O.CS(N)(=O)=O.[CH3:36][S:37]([NH:40][C:41](=[O:63])[C:42]1[CH:47]=[C:46]([O:48][C:49]2[CH:54]=[C:53]([C:55]([F:58])([F:57])[F:56])[CH:52]=[CH:51][C:50]=2[Cl:59])[CH:45]=[CH:44][C:43]=1[N+]([O-])=O)(=[O:39])=[O:38]>N1C=CC=CC=1>[CH3:36][S:37]([NH:40][C:41](=[O:63])[C:42]1[CH:43]=[CH:44][CH:45]=[C:46]([O:48][C:49]2[CH:54]=[C:53]([C:55]([F:58])([F:57])[F:56])[CH:52]=[CH:51][C:50]=2[Cl:59])[CH:47]=1)(=[O:38])=[O:39]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 24386Thionyl ChlorideHCID 72879MethanesulfonamideHCID 21287078Methyl 5-(2-amino-6-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoateHCID 212870795-[2-chloro-5-(trifluoromethyl)phenoxy]-N-methanesulfonyl-2-nitrobenzamide

생성물 1

HCID 21287082N-methane-sulphonyl-3-(2-chloro-5-trifluoromethylphenoxy)benzamide

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

The acid from (b) (0.8 g) was treated with thionyl chloride followed by methanesulphonamide and pyridine as described in paragraph (d) above for compound 32. The product was recrystallised from a mixture of ether and petroleum (b.p. 40°-60°) to give compound 31 with a melting point of 132°-133°.

후처리

  1. customThe product was recrystallised from a mixture of ether and petroleum (b.p. 40°-60°)

출처 및 근거

ORD 기록
ord-2b42f58b0a8f4fe9a76680de0ac5b5c8
출처 데이터셋
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04738711

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