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Benzylamine → 4-N-benzyl-2-N-(4-methoxyphenyl)pyridine-2,4-diamine

HRID 531
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HRID 531 반응식
COc1ccc(Nc2cc(Cl)ccn2)cc1.NCc1ccccc1>C1CCCC1.CC(=O)N(C)C.CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C1CCCC1P(C1CCCCC1)C1CCCCC1)P(C(C)(C)C)C(C)(C)C.[Fe].[Na+].[Pd]>COc1ccc(Nc2cc(NCc3ccccc3)ccn2)cc1
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참가 물질

7

반응물 2

HCID 7504BenzylamineHCID 1022185114-chloro-N-(4-methoxyphenyl)pyridin-2-amine

생성물 1

HCID 1018836904-N-benzyl-2-N-(4-methoxyphenyl)pyridine-2,4-diamine수율 59.17%

시약·촉매·용매 4

HCID 23676156Sodium t-butoxide시약HCID 4144353Palladium (II) acetate촉매
HCID 144543273
(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-
촉매
HCID 31374Dimethylacetamide용매

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온도
100 °C

실험 절차

Phenylmethanamine (50.2 mg, 0.47 mmol), 4-chloro-N-(4-methoxyphenyl)pyridin-2-amine (100 mg, 0.43 mmol) and sodium 2-methylpropan-2-olate (82 mg, 0.85 mmol) were suspended in DMA (2 mL) and sealed into a microwave tube. Nitrogen was bubbled through the reaction mixture for 5 minutes. (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (28.4 mg, 0.05 mmol) and diacetoxypalladium (7.65 mg, 0.03 mmol) were added to the reaction mixture and nitrogen was bubbled through the reaction mixture for a further 5 minutes. The reaction was heated thermally to 100 °C for 30 mins under nitrogen and cooled to RT. The reaction mixture was neutralised with HCl and purified by ion exchange chromatography, using a 20 g SCX column. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% MeOH in DCM. Fractions containing product were evaporated to dryness to afford N4-benzyl-N2-(4-methoxyphenyl)pyridine-2,4-diamine (77 mg, 59.2 %) as an off-white solid.

출처 및 근거

ORD 기록
ord-1c5be4d17d4d4231816c56243b381f3c
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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