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Bromine → HCID 10524413, 화합물

HRID 724933
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HRID 724933 반응식
[Cl:1][C:2]1[C:7]([NH:8][C:9]([C:11]2[C:12]([NH:17][CH2:18][CH3:19])=[N:13][CH:14]=[CH:15][CH:16]=2)=[O:10])=[CH:6][CH:5]=[C:4]([Cl:20])[N:3]=1.C([O-])(=O)C.[K+].[Br:26]Br>C(O)(=O)C.O>[Cl:1][C:2]1[C:7]([NH:8][C:9]([C:11]2[C:12]([NH:17][CH2:18][CH3:19])=[N:13][CH:14]=[C:15]([Br:26])[CH:16]=2)=[O:10])=[CH:6][CH:5]=[C:4]([Cl:20])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 24408BromineHCID 517044Potassium AcetateHCID 10828808N-(2,6-Dichloro-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide

생성물 1

HCID 10524413HCID 10524413, 화합물수율 91.4%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

실험 절차

To a solution of N-(2,6-dichloro-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide (7.4 g, 24 mmol) and potassium acetate (2.8 g, 28 mmol) in 90 mL of acetic acid was added bromine (1.2 mL, 23 mmol). After 15 min, the reaction mixture was diluted with water and the precipitate was collected by suction filtration to give 8.2 g of the title compound, suitable for use in the next reaction.

후처리

  1. filtrationthe precipitate was collected by suction filtration

출처 및 근거

ORD 기록
ord-6e0dd69969e54a58bc9d14da8ee9e638
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05705499

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