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Sodium Carbonate → 1-Amino-7-phenyl[1]benzothieno[3,2-c]pyridine-4-carboxamide

HRID 1896537
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HRID 1896537 반응식
[NH2:1][C:2]1[C:7]2[C:8]3[CH:14]=[CH:13][C:12](Br)=[CH:11][C:9]=3[S:10][C:6]=2[C:5]([C:16]([NH2:18])=[O:17])=[CH:4][N:3]=1.[C:19]1(B(O)O)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C([O-])([O-])=O.[Na+].[Na+]>CN(C=O)C>[NH2:1][C:2]1[C:7]2[C:8]3[CH:14]=[CH:13][C:12]([C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)=[CH:11][C:9]=3[S:10][C:6]=2[C:5]([C:16]([NH2:18])=[O:17])=[CH:4][N:3]=1
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참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 66827Phenylboronic AcidHCID 235819291-Amino-7-bromo[1]benzothieno[3,2-c]pyridine-4-carboxamide

생성물 1

HCID 235819981-Amino-7-phenyl[1]benzothieno[3,2-c]pyridine-4-carboxamide

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a suspension of 1-amino-7-bromo[1]benzothieno[3,2-c]pyridine-4-carboxamide (Example 12, Step 10) in DMF (0.1 M) was added phenylboronic acid (1.5 equiv). The mixture was degassed for 5 min, and 1 M Na2CO3 (3 equiv) and PdCl2dppf (0.1 equiv) were added. It was heated is the microwave reactor at 120° C. for 10 min. The reaction mixture was partitioned between EtOAc and H2O. The organic phase was separated, dried over MgSO4, filtered, evaporated and purified by flash chromatography (EtOAc/MeOH) to provide the title compound.

후처리

  1. customThe mixture was degassed for 5 min
  2. temperatureIt was heated
  3. customat 120° C.
  4. customfor 10 min
  5. customThe reaction mixture was partitioned between EtOAc and H2O
  6. customThe organic phase was separated
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. customevaporated
  10. custompurified by flash chromatography (EtOAc/MeOH)

출처 및 근거

ORD 기록
ord-891c0468fc5e40d48eb749d2d12181c4
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08518964B2

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