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Ammonia → HCID 22663070, 화합물

HRID 1593511
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HRID 1593511 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[N:7][CH:8]=2)[CH:3]=[CH:2]1.C[Mg]I.[C:13](Cl)(=[O:17])[C:14](Cl)=[O:15].[N:19]1C=CC=CC=1.N>CCOCC.[Cl-].[Zn+2].[Cl-]>[O:15]=[C:14]([C:3]1[C:4]2[C:9](=[CH:8][N:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1)[C:13]([NH2:19])=[O:17]
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참가 물질

8

반응물 5

HCID 222AmmoniaHCID 1049PyridineHCID 92196-AzaindoleHCID 65578Oxalyl chlorideHCID 178418373HCID 178418373, 화합물

생성물 1

HCID 22663070HCID 22663070, 화합물

시약·촉매·용매 2

HCID 3007855
Zincchloride
촉매
HCID 3283Diethyl Ether용매

실험 절차

A solution of 6-azaindole (1.0 eq.) in ether is treated with methyl magnesium iodide (1.1 eq.) at room temperature, stirred for 1 h, treated with zinc chloride (1.2 eq), stirred for a further 1 h, treated with oxalyl chloride (10 eq.), stirred for 10 h and concentrated in vacuo to remove the solvent and excess oxalyl chloride. The resultant residue is dissolved in CH3CN and pyridine (1.6 eq.), treated with ammonia (2 eq., solution in dioxane), stirred for 1 h and concentrated in vacuo. This residue is purified by chromatography [silica gel, CH2Cl2/methanol (containing 5% ammonium hydroxide) as eluent] to afford the title acetamide compound.

후처리

  1. stirringstirred for a further 1 h
  2. stirringstirred for 10 h
  3. concentrationconcentrated in vacuo
  4. customto remove the solvent and excess oxalyl chloride
  5. dissolutionThe resultant residue is dissolved in CH3CN
  6. stirringstirred for 1 h
  7. concentrationconcentrated in vacuo
  8. customThis residue is purified by chromatography [silica gel, CH2Cl2/methanol (containing 5% ammonium hydroxide) as eluent]

출처 및 근거

ORD 기록
ord-d9b5fe4965834393827e09c170b6d582
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07297705B2

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