Dimethylamine → N4,N4,6-Trimethyl-2,4-pyridinediamine

反応式

[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[CH:5]=[C:4](Cl)[CH:3]=1.[CH3:10][NH:11][CH3:12]>>[CH3:10][N:11]([CH3:12])[C:4]1[CH:5]=[C:6]([CH3:8])[N:7]=[C:2]([NH2:1])[CH:3]=1

参加物

反応物 2

HCID 674Dimethylamine

HCID 190505094-Chloro-6-methylpyridin-2-amine

生成物 1

HCID 667547N4,N4,6-Trimethyl-2,4-pyridinediamine

反応条件

温度: 130 °C

実験手順

To 6-amino-4-chloro-2-picoline (500 mg, 3.51 mmol) in a vial under nitrogen was added dimethylamine (40% in water, 17.5 ml, 35.0 mmol). The reaction mixture was sealed and heated at 130° C. in a microwave for 2.5 hours. The reaction mixture was cooled, concentrated under reduced pressure, and purified by silica gel chromatography (2-10% methanol/DCM with 1% ammonium hydroxide, linear gradient) to give N4,N4,6-trimethylpyridine-2,4-diamine. MS ESI calc'd. for C8H14N3 [M+H]+ 152. found 152. 1H NMR (500 MHz, DMSO-d6) δ 6.15 (s, 2H), 6.02 (s, 1H), 5.54 (s, 1H), 2.90 (s, 6H), 2.18 (s, 3H).

後処理

customThe reaction mixture was sealed
temperatureThe reaction mixture was cooled
concentrationconcentrated under reduced pressure
custompurified by silica gel chromatography (2-10% methanol/DCM with 1% ammonium hydroxide, linear gradient)

出典と根拠

ORDレコード: ord-be7d9f75d3f14dc0aa52d055fcf08d76
出典データセット: uspto-grants-2015_12
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US09216173B2

反応ノート

読み込み中…

参加物