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

HRID 603
ノート
印刷プレビュー

反応式

HRID 603 の反応式
Clc1ccnc(Nc2ccccc2)c1.NCc1ccncc1>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]>c1ccc(Nc2cc(NCc3ccncc3)ccn2)cc1
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 773174-PyridinemethanamineHCID 234580414-chloro-N-phenylpyridin-2-amine

生成物 1

HCID 1018836992-N-phenyl-4-N-(pyridin-4-ylmethyl)pyridine-2,4-diamine収率 23.11%

試薬・触媒・溶媒 4

HCID 23676156Sodium t-butoxide試薬HCID 4144353Palladium (II) acetate触媒
HCID 144543273
(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-
触媒
HCID 31374Dimethylacetamide溶媒

反応条件

温度
100 °C

実験手順

Pyridin-4-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 impure product. Impure product was purified by flash silica chromatography, elution gradient 3 to 8% MeOH in DCM. Fractions containing product were evaporated to dryness to afford impure product. Impure product was purified by preparative HPLC (Waters SunFire column, 5µ silica, 50 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 0.1% formic acid) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness N2-phenyl-N4-(pyridin-4-ylmethyl)pyridine-2,4-diamine (31.2 mg, 23.11 %) as an off white solid.

出典と根拠

ORDレコード
ord-63fc87ded08344459c39e54d90416da8
出典データセット
750 AstraZeneca ELN dataset
元リンク
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反応ノート

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