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Sodium Carbonate → 3-Nitro-6-chloro-N-(thiazolo[4,5-c]pyridin-2-ylmethyl)pyridin-2-amine

HRID 1890595
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HRID 1890595 반응식
[N+:1]([C:4]1[C:5](Cl)=[N:6][C:7]([Cl:10])=[CH:8][CH:9]=1)([O-:3])=[O:2].C([O-])([O-])=O.[Na+].[Na+].[S:18]1[C:26]2[CH:25]=[CH:24][N:23]=[CH:22][C:21]=2[N:20]=[C:19]1[CH2:27][NH2:28]>C(O)(C)C>[N+:1]([C:4]1[C:5]([NH:28][CH2:27][C:19]2[S:18][C:26]3[CH:25]=[CH:24][N:23]=[CH:22][C:21]=3[N:20]=2)=[N:6][C:7]([Cl:10])=[CH:8][CH:9]=1)([O-:3])=[O:2]
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참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 852392,6-Dichloro-3-nitropyridineHCID 65441030Thiazolo[4,5-c]pyridine-2-methanamine

생성물 1

HCID 866714403-Nitro-6-chloro-N-(thiazolo[4,5-c]pyridin-2-ylmethyl)pyridin-2-amine

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a solution of 3-nitro-2,6-dichloropyridine (106 mg, 0.55 mmol) in isopropanol (3 mL) was sequentially added Na2CO3 (116 mg, 1.1 mmol) and intermediate R (100 mg, 0.61 mmol). The reaction mixture was stirred at room temperature overnight, and then concentrated. The residue was extracted with EtOAc. The organic layer was separated, concentrated, and purified by chromatography on silica gel to afford the title compound. MS (m/z): 322 (M)+.

후처리

  1. concentrationconcentrated
  2. extractionThe residue was extracted with EtOAc
  3. customThe organic layer was separated
  4. concentrationconcentrated
  5. custompurified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-a9877dc3c3c24326a5514c0dddc70b26
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507487B2

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