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Benzylamine → 4-N-benzyl-2-N-phenylpyridine-2,4-diamine

HRID 537
ノート
印刷プレビュー

反応式

HRID 537 の反応式
Clc1ccnc(Nc2ccccc2)c1.NCc1ccccc1>CC(=O)N(C)C.CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.[Na+].[Pd]>c1ccc(CNc2ccnc(Nc3ccccc3)c2)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 7504BenzylamineHCID 234580414-chloro-N-phenylpyridin-2-amine

生成物 1

HCID 1018836884-N-benzyl-2-N-phenylpyridine-2,4-diamine収率 13.23%

試薬・触媒・溶媒 4

HCID 23676156Sodium t-butoxide試薬HCID 4144353Palladium (II) acetate触媒
HCID 16217985
2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl
触媒
HCID 31374Dimethylacetamide溶媒

反応条件

温度
100 °C

実験手順

Phenylmethanamine (57.6 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. 2-Dicyclohexylphosphino-2',6'-di- i-propoxy-1,1'-biphenyl (27.4 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 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 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 N4-benzyl-N2-phenylpyridine-2,4-diamine (17.80 mg, 13.23 %) as an off-white solid.

出典と根拠

ORDレコード
ord-6ec08990002f44da89217320c1b9e8f7
出典データセット
750 AstraZeneca ELN dataset
元リンク
出典を表示

反応ノート

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