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Iodine → HCID 68283346, 화합물

HRID 1527312
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HRID 1527312 반응식
[NH:1]1[C:5]2=[N:6][N:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[N:2]1.[I:10]I.[OH-].[K+].Br[CH2:15][C:16]([O:18][CH3:19])=[O:17]>CN(C=O)C.CCOC(C)=O>[I:10][C:3]1[C:4]2[C:5](=[N:6][N:7]=[CH:8][CH:9]=2)[N:1]([CH2:15][C:16]([O:18][CH3:19])=[O:17])[N:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 807IodineHCID 14797Potassium HydroxideHCID 60984Methyl bromoacetateHCID 219482541H-Pyrazolo[3,4-c]pyridazine

생성물 1

HCID 68283346HCID 68283346, 화합물

시약·촉매·용매 2

HCID 6228Dimethylformamide용매
HCID 8857
Ethyl Acetate
용매

실험 절차

To a solution of 1H-pyrazolo[3,4-c]pyridazine [271-75-0] (450 mg, 3.75 mmol) in DMF (10 mL) was added iodine (951 mg, 3.75 mmol) and KOH (525 mg, 9.37 mmol). The mixture was stirred at RT for 16 h until completion of the reaction. Methyl 2-bromoacetate (0.380 mL, 4.12 mmol) was then added to the reaction mixture and stirring was continued at RT for 2 h. The mixture was diluted with EtOAc and washed with water (10 mL), the organic phase was dried (Na2SO4) and evaporated under vacuum. The crude mixture was purified by flash column chromatography on silica gel (c-Hex/EtOAc 66:33) to afford the title compound as a brown solid. TLC, Rf (c-Hex/EtOAc 1:1)=0.40; MS (LC/MS): 318.9 [M+H]+; tR (HPLC conditions c): 3.35 min.

후처리

  1. stirringstirring
  2. waitwas continued at RT for 2 h
  3. washwashed with water (10 mL)
  4. dry with materialthe organic phase was dried (Na2SO4)
  5. customevaporated under vacuum
  6. customThe crude mixture was purified by flash column chromatography on silica gel (c-Hex/EtOAc 66:33)

출처 및 근거

ORD 기록
ord-204ed26650a94b82bf2faacb26082c88
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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