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1,1-Dimethoxyethyl(dimethyl)amine → 3-(2-Bromo-4-chloro-6-fluorophenyl)-5-methyl-1,2,4-oxadiazole

HRID 1404556
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HRID 1404556 반응식
[Br:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]([F:13])[C:3]=1[C:4]([NH:6][OH:7])=[NH:5].CO[C:16](OC)(N(C)C)[CH3:17]>CC(O)C>[Br:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]([F:13])[C:3]=1[C:4]1[N:5]=[C:16]([CH3:17])[O:7][N:6]=1
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참가 물질

4

반응물 2

HCID 878351,1-Dimethoxyethyl(dimethyl)amineHCID 178513381HCID 178513381, 화합물

생성물 1

HCID 684506413-(2-Bromo-4-chloro-6-fluorophenyl)-5-methyl-1,2,4-oxadiazole수율 95.1%

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a solution of 2-bromo-4-chloro-6-fluoro-N-hydroxy-benzamidine (26.5 g, 99.25 mmol) in 2-propanol (200 ml) was added N,N-dimethylacetamide dimethyl acetal (35.2 ml, 238.20 mmol) slowly at 25° C. and the reaction mixture was stirred for 30 minutes. After completion of the reaction all volatiles were evaporated and the resulting crude product was purified by chromatography (silica gel; hexane/EtOAc 97:3) to obtain the title compound as white solid (27.5 g, 58%). MS: m/z=290 [M]+.

후처리

  1. customAfter completion of the reaction all volatiles
  2. customwere evaporated
  3. customthe resulting crude product was purified by chromatography (silica gel; hexane/EtOAc 97:3)

출처 및 근거

ORD 기록
ord-86fcf8362b6147c5a7a3f9f7e48e21ac
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08912221B2

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