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2-Chloropyrimidine → N-[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]pyrimidin-2-amine

HRID 257
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HRID 257 반응식
COc1cc(N)ccc1-n1cnc(C)c1.Clc1ncccn1>CC(=O)O.CC(=O)O.COCCOC.O=C([O-])[O-].[Cs+].[Cs+].[Pd].c1ccc(-c2ccccc2P(C2CCCCC2)C2CCCCC2)cc1>COc1cc(Nc2ncccn2)ccc1-n1cnc(C)c1
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참가 물질

7

반응물 2

HCID 744042-ChloropyrimidineHCID 454801813-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline

생성물 1

HCID 68790359N-[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]pyrimidin-2-amine수율 18.78%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 27342162-(Dicyclohexylphosphino)biphenyl촉매
HCID 4144353
Palladium (II) acetate
촉매
HCID 80711,2-Dimethoxyethane용매

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온도
100 °C

실험 절차

2-Chloropyrimidine (0.056 g, 0.49 mmol), 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline (0.100 g, 0.49 mmol), Palladium acetate (0.011 g, 0.05 mmol), 2-(Dicyclohexylphosphino)biphenyl (0.017 g, 0.05 mmol) and Cesium carbonate (0.481 g, 1.48 mmol) were placed in a microwave vial. The mixture was capped and flushed with argon. 1,2-dimethoxyethane (5 mL) was added and the mixture was run in a microwave for 60 minutes at 100°C. Very little product. Added 0.1 eq ligand and palladium acetate, flushed with argon and run in the microwave at 100°C for 60 min. No change. Seems as if the 2-chloropyrimidine is not very soluble in DME. Added 1.5 mL DMF and the reaction was run again in the microwave for 60 minutes. The reaction mixture was filtrated through Celite and washed with dichloromethane. The filtrate was concentrated and the crude product was purified by preparative chromatography. The productcontaining fractions were pooled, concentrated and the residue was partitioned between sat. NaHCO3 (aq) and dichloromethane. The organic layer was separated by a Phase Separator and concentrated giving N-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)pyrimidin-2-amine (0.026 g, 18.78 %).

출처 및 근거

ORD 기록
ord-20ba80f324544fc48cbce515702585f3
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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