Ethylamine → N-ethyl-5-(6-methoxy-1,3-benzothiazol-2-yl)pyridin-2-amine

HRID 1698082ノート

反応式

HRID 1698082 の反応式
F[C:2]1[N:7]=[CH:6][C:5]([C:8]2[S:9][C:10]3[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:11]=3[N:12]=2)=[CH:4][CH:3]=1.[CH2:19]([NH2:21])[CH3:20]>O>[CH2:19]([NH:21][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[S:9][C:10]3[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:11]=3[N:12]=2)=[CH:6][N:7]=1)[CH3:20]

参加物

4

反応物 2

HCID 6341EthylamineHCID 248037222-(6-Fluoropyridin-3-yl)-6-methoxy-1,3-benzothiazole

生成物 1

HCID 24803887N-ethyl-5-(6-methoxy-1,3-benzothiazol-2-yl)pyridin-2-amine

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

反応条件

温度
100 °C

実験手順

In a microwave vial were added 2-(6-fluoropyridin-3-yl)-6-methoxy-1,3-benzothiazole (75 mg, 0.289 mmol), water (1.2 mL) and ethylamine in water (70%, 1.2 mL) and the reaction was heated in a microwave oven at 100° C. for 5 min. The precipitated product was filtered off, washed with water and dried in a desicator over P2O5 to yield the product (67 mg) as a white solid. 1H NMR δ ppm 8.62 (d, 1H) 7.95 (dd, 1H) 7.82 (d, 1H) 7.64 (d, 1H) 7.23 (t, 1H) 7.07 (dd, 1H) 6.57 (d, 1H) 3.83 (s, 3H) 3.33-3.40 (m, 2H) 1.16 (t, 3H); MS m/z (M+H) 286.

後処理

  1. filtrationThe precipitated product was filtered off
  2. washwashed with water
  3. dry with materialdried in a desicator over P2O5

出典と根拠

ORDレコード
ord-294fb01ec83240d1924c1127d6ee9e3e
出典データセット
uspto-grants-2012_04
特許番号
US08163928B2

反応ノート

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