Ethyl imino(2-bromopyridin-5-yl)acetate → 2-bromo-5-[(1, 3-dibutyl-1H-1,2,4-triazol-5-yl)methyl]pyridine

HRID 2399757ノート

反応式

HRID 2399757 の反応式
N=[C:2]([C:8]1[CH:9]=[CH:10][C:11]([Br:14])=[N:12][CH:13]=1)[C:3](OCC)=O.[N:15]#[N:16].C([CH:21]([CH2:26][CH2:27][CH3:28])[C:22]([NH:24]N)=O)CCC>CO>[Br:14][C:11]1[CH:10]=[CH:9][C:8]([CH2:2][C:3]2[N:16]([CH2:3][CH2:2][CH2:8][CH3:13])[N:15]=[C:22]([CH2:21][CH2:26][CH2:27][CH3:28])[N:24]=2)=[CH:13][N:12]=1

参加物

4

反応物 2

HCID 53879744Ethyl imino(2-bromopyridin-5-yl)acetateHCID 86746659HCID 86746659、化合物

生成物 1

HCID 152912752-bromo-5-[(1, 3-dibutyl-1H-1,2,4-triazol-5-yl)methyl]pyridine収率 79.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Under nitrogen, a solution of 1.2 g (5 mmol) of imidate ester from step 6 and 850 mg (5 mmol) of N2 -butyl valeric acid hydrazide from step 2 in 25 mL of absolute methanol was stirred for 24 h at ambient temperature. The methanol was removed in vacuo and replaced with 25 mL of anhydrous toluene. The reaction vessel was equipped with a Dean-Stark trap and the reaction stirred at reflux for 48 h. Concentration in vacuo produced the crude product residue. Purification by silica gel chromatography (Waters Prep-500A) using ethyl acetate/hexane (60:40) gave 700 mg (40%) of 2-bromo-5-[(1, 3-dibutyl-1H-1,2,4-triazol-5-yl)methyl]pyridine as an oil: NMR (CDCl3) δ 0.88 (t, J=7Hz, 3H), 0.92 (t, J=7Hz, 3H), 1.25-1.75 (m, 8H), 2.67 (t, J=8Hz, 2H), 3.93 (t, J= 7Hz, 2H), 4.05 (s, 2H), 7.43 (s, 1H), 7.44 (s, 1H), 8.27 (s, 1H); MS (FAB)m/e (rel intensity) 353 (50), 351 (50), 297 (100), 295 (100), 215 (40), 160 (90), 158 (90), 138 (70).

後処理

  1. customThe methanol was removed in vacuo
  2. customThe reaction vessel was equipped with a Dean-Stark trap
  3. temperatureat reflux for 48 h
  4. concentrationConcentration in vacuo
  5. customproduced the crude product residue
  6. customPurification by silica gel chromatography (Waters Prep-500A)

出典と根拠

ORDレコード
ord-e8f33ebd2e4a4857a6f5f3cc690e68f7
出典データセット
uspto-grants-1995_09
特許番号
US05451591

反応ノート

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