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Potassium Carbonate → HCID 69284611, 화합물

HRID 332839
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HRID 332839 반응식
Br[C:2]1[N:7]=[CH:6][CH:5]=[CH:4][N:3]=1.Cl.[NH2:9][C:10]1[CH:11]=[C:12](B(O)O)[CH:13]=[N:14][CH:15]=1.C([O-])([O-])=O.[K+].[K+]>O1CCOCC1.O.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[N:3]1[CH:4]=[CH:5][CH:6]=[N:7][C:2]=1[C:12]1[CH:11]=[C:10]([NH2:9])[CH:15]=[N:14][CH:13]=1
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참가 물질

7

반응물 3

HCID 11430Potassium CarbonateHCID 783452-BromopyrimidineHCID 53398527(5-Aminopyridin-3-yl)boronic acid hydrochloride

생성물 1

HCID 69284611HCID 69284611, 화합물수율 29%

시약·촉매·용매 3

HCID 178418476HCID 178418476, 화합물촉매HCID 962
Water
용매
HCID 312751,4-Dioxane용매

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온도
95 °C

실험 절차

The mixture of 2-bromopyrimidine (0.76 g, 4.80 mmol), (5-aminopyridin-3-yl)boronic acid hydrochloride (1.00 g, 5.75 mmol), Pd(Ph3P)2Cl2 (0.73 g, 0.96 mmol) and K2CO3 (2.78 g, 20.2 mmol) in dioxane (40 mL) and water (10 mL) was degassed with argon stream. It was stirred at 95° C. in argon atmosphere for overnight. The mixture was concentrated in vacuo to dryness. The solid was triturated with dioxane and EtOAc. The organic solutions were combined, filtered, concentrated and subjected to flash column (0-8% MeOH in DCM) to isolate 5-(pyrimidin-2-yl)pyridin-3-amine (0.24 g).

후처리

  1. customwas degassed with argon stream
  2. concentrationThe mixture was concentrated in vacuo to dryness
  3. customThe solid was triturated with dioxane and EtOAc
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-208f30bae47c4417af95c423836c89d2
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877760B2

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