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Water → 5-Cyano-2,3'-bipyridine-6'-carboxylic acid

HRID 2098454
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HRID 2098454 반응식
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([C:9]2[CH:10]=[N:11][C:12]([C:15]([O:17]C)=[O:16])=[CH:13][CH:14]=2)=[N:7][CH:8]=1)#[N:2].O.[Li+].[OH-]>O1CCCC1>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([C:9]2[CH:10]=[N:11][C:12]([C:15]([OH:17])=[O:16])=[CH:13][CH:14]=2)=[N:7][CH:8]=1)#[N:2]
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참가 물질

5

반응물 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 58286497Methyl 5-cyano-2,3'-bipyridine-6'-carboxylate

생성물 1

HCID 582865945-Cyano-2,3'-bipyridine-6'-carboxylic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a 250 ml flask was added methyl 5-cyano-2,3′-bipyridine-6′-carboxylate (950 mg, 3.57 mmol), water (9.5 ml), tetrahydrofuran (38.4 ml) and LiOH (86 mg, 3.57 mmol). The mixture was stirred for 30 min, diluted with tetrahydrofuran (200 ml) and cooled to 0° C. (ice water batch). After an additional 30 min, the resulting suspension was filtered, washed with THF and dried under reduced pressure to afford the desired product as a light brown powder. LCMS (m/z): 226.1 (M+H).

후처리

  1. waitAfter an additional 30 min
  2. filtrationthe resulting suspension was filtered
  3. washwashed with THF
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-b999a10f9a604241b5d1d6d500c4f2a8
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450484B2

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