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Potassium Phosphate, Tribasic → Methyl 2-(4-(4-(2-aminopyrimidin-5-yl)phenyl)-2-oxabicyclo[2.2.2]octan-1-yl)acetate

HRID 881721
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HRID 881721 반응식
CC1(C)C(C)(C)OB([C:9]2[CH:14]=[CH:13][C:12]([C:15]34[CH2:22][CH2:21][C:18]([CH2:23][C:24]([O:26][CH3:27])=[O:25])([CH2:19][CH2:20]3)[O:17][CH2:16]4)=[CH:11][CH:10]=2)O1.Br[C:30]1[CH:31]=[N:32][C:33]([NH2:36])=[N:34][CH:35]=1.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl.C(COC)OC>[NH2:36][C:33]1[N:34]=[CH:35][C:30]([C:9]2[CH:10]=[CH:11][C:12]([C:15]34[CH2:22][CH2:21][C:18]([CH2:23][C:24]([O:26][CH3:27])=[O:25])([CH2:19][CH2:20]3)[O:17][CH2:16]4)=[CH:13][CH:14]=2)=[CH:31][N:32]=1
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참가 물질

6

반응물 3

HCID 62657Potassium Phosphate, TribasicHCID 2313102-Amino-5-bromopyrimidineHCID 86700826Methyl 2-(4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-oxabicyclo[2.2.2]octan-1-yl)acetate

생성물 1

HCID 86700829Methyl 2-(4-(4-(2-aminopyrimidin-5-yl)phenyl)-2-oxabicyclo[2.2.2]octan-1-yl)acetate수율 105%

시약·촉매·용매 2

HCID 178418807
HCID 178418807, 화합물
촉매
HCID 80711,2-Dimethoxyethane용매

실험 절차

To a reaction vial containing methyl 2-(4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-oxabicyclo[2.2.2]octan-1-yl)acetate (200 mg, 0.52 mmol), 5-bromopyrimidin-2-amine (108 mg, 0.62 mmol) and K3PO4 (132 mg, 0.62 mmol) was added dimethoxyethane (4.8 ml). The mixture was stirred at room temperature and degassed after the addition of EtOH (1.6 ml) and water (0.64 ml). PdCl2(dppf) DCM adduct (21 mg, 0.03 mmol) was added and the mixture was heated to 8° C. in an oil bath for 3 hours. The reaction mixture was then concentrated to dryness and taken up in DCM. The slurry was dried over sodium sulfate and filtered through a pad of celite. The filtrate was concentrated and purified by column chromatography to afford the title compound (193 mg, 84% yield). LC/MS, ESI-MS(+): 354.3, RT: 1.06 (Condition E).

후처리

  1. customdegassed
  2. additionafter the addition of EtOH (1.6 ml) and water (0.64 ml)
  3. temperaturethe mixture was heated to 8° C. in an oil bath for 3 hours
  4. concentrationThe reaction mixture was then concentrated to dryness
  5. dry with materialThe slurry was dried over sodium sulfate
  6. filtrationfiltered through a pad of celite
  7. concentrationThe filtrate was concentrated
  8. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-d12e49ad3c3f44db926dc759c7afa167
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993619B2

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