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Hydrochloric Acid → HCID 67363585, 화합물

HRID 1183184
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HRID 1183184 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:9]=[C:8]([O:10][CH3:11])[N:7]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[F:18])[N:6]=1)=[O:4].[F:19][B-](F)(F)F.F[B-](F)(F)F.Cl[N+]12CC[N+](F)(CC1)CC2C.C(OCC)C.Cl>C(#N)C.O>[CH3:1][O:2][C:3]([C:5]1[C:9]([F:19])=[C:8]([O:10][CH3:11])[N:7]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[F:18])[N:6]=1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 67363124HCID 67363124, 화합물HCID 178429830HCID 178429830, 화합물

생성물 1

HCID 67363585HCID 67363585, 화합물수율 33%

시약·촉매·용매 2

HCID 962Water용매
HCID 6342
Acetonitrile
용매

실험 절차

200 mg (0.8 mmol) of 1-(2-fluoro-phenyl)-5-methoxy-1H-pyrazole-3-carboxylic acid methyl ester were dissolved in 2 ml of acetonitrile and 745 mg (1.99 mmol) of 1-chloro-methyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor®) were added. The mixture was stirred overnight. Then, irrespective of the incomplete reaction, diethyl ether, water and 2 N hydrochloric acid were added, the organic phase was separated, the solvent evaporated and the residue subjected to preparative HPLC. 70 mg (33%) of the title compound were obtained.

후처리

  1. additionwere added
  2. customthe organic phase was separated
  3. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-e4c1a94de74d4cc49eda661390f6c929
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664257B2

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