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3-Pyridinemethanamine → 2-N-phenyl-4-N-(pyridin-3-ylmethyl)pyridine-2,4-diamine

HRID 525
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인쇄 미리보기

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HRID 525 반응식
Clc1ccnc(Nc2ccccc2)c1.NCc1cccnc1>C1CCCC1.CC(=O)N(C)C.CC(C)(C)[O-].CC(C1CCCC1P(C1CCCCC1)C1CCCCC1)P(C(C)(C)C)C(C)(C)C.[Fe].[Na+]>c1ccc(Nc2cc(NCc3cccnc3)ccn2)cc1
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참가 물질

6

반응물 2

HCID 310183-PyridinemethanamineHCID 234580414-chloro-N-phenylpyridin-2-amine

생성물 1

HCID 1018836932-N-phenyl-4-N-(pyridin-3-ylmethyl)pyridine-2,4-diamine수율 59.25%

시약·촉매·용매 3

HCID 23676156Sodium t-butoxide시약
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

Pyridin-3-ylmethanamine (58.1 mg, 0.54 mmol), 4-chloro-N-phenylpyridin-2-amine (100 mg, 0.49 mmol) and sodium 2-methylpropan-2-olate (94 mg, 0.98 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 (32.5 mg, 0.06 mmol) and diacetoxypalladium (8.78 mg, 0.04 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 N2-phenyl-N4-(pyridin-3-ylmethyl)pyridine-2,4-diamine (80 mg, 59.2 %) as an off white solid.

출처 및 근거

ORD 기록
ord-4389cfc2af664ae3968b09023440510c
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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