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Ethanol, 2-(aminooxy)- → HCID 89451604、化合物

HRID 2175154
ノート
印刷プレビュー

反応式

HRID 2175154 の反応式
Cl.[O:2]1[CH2:7][CH2:6][N:5]([CH2:8][C:9]2[CH:10]=[N:11][C:12]3[C:17]([CH:18]=2)=[CH:16][C:15]([S:19][C:20]2[N:24]4[CH:25]=[C:26]([C:29](=O)[CH3:30])[CH:27]=[CH:28][C:23]4=[N:22][N:21]=2)=[CH:14][CH:13]=3)[CH2:4][CH2:3]1.[NH2:32][O:33][CH2:34][CH2:35][OH:36]>CO.Cl>[OH:36][CH2:35][CH2:34][O:33]/[N:32]=[C:29](/[C:26]1[CH:27]=[CH:28][C:23]2[N:24]([C:20]([S:19][C:15]3[CH:16]=[C:17]4[C:12](=[CH:13][CH:14]=3)[N:11]=[CH:10][C:9]([CH2:8][N:5]3[CH2:6][CH2:7][O:2][CH2:3][CH2:4]3)=[CH:18]4)=[N:21][N:22]=2)[CH:25]=1)\[CH3:30]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 3014186Ethanol, 2-(aminooxy)-HCID 86696281HCID 86696281、化合物

生成物 1

HCID 89451604HCID 89451604、化合物収率 54.2%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid触媒HCID 887Methanol溶媒

反応条件

温度
85 °C

実験手順

To a solution of 1-(3-(3-(morpholinomethyl)quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)ethanone hydrochloride (79.3) (23 mg, 0.047 mmol) and 2-(aminooxy)ethanol (10.80 mg, 0.140 mmol) in MeOH (5 ml) was added 2 drops of HCl (2 N) by a 1-ml syringe to reach pH about 3 and the mixture was stirred in a sealed tube at 85° C. for 3 h. The mixture was evaporated to dryness and the residue was dissolved in water. The solution was neutralized by adding solid NaHCO3 until pH reached 9, then extracted by DCM (3×). The combined organic layers were washed by water again, dried over Na2SO4, filtered and evaporated. The residue was purified by preparative base HPLC (gradient eluent NB from 20/80 to 95/5. mobile phase A: NH4OH/CH3CN 0.04%; mobile phase B: NH4OH/H2O 0.04%). The desired fractions were collected, evaporated by BUCHI under 30 mbar at 35° C. to remove CH3CN. The remained solution was lyophilized to afford the title compound (12.2 mg, yield 54.2%).

後処理

  1. customThe mixture was evaporated to dryness
  2. dissolutionthe residue was dissolved in water
  3. additionby adding solid NaHCO3 until pH
  4. extractionextracted by DCM (3×)
  5. washThe combined organic layers were washed by water again
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was purified by preparative base HPLC (gradient eluent NB from 20/80 to 95/5. mobile phase A: NH4OH/CH3CN 0.04%; mobile phase B: NH4OH/H2O 0.04%)
  10. customThe desired fractions were collected
  11. customevaporated by BUCHI under 30 mbar at 35° C.
  12. customto remove CH3CN

出典と根拠

ORDレコード
ord-ccd8028640ae46a9a20111f4c1bb0550
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09062045B2

反応ノート

読み込み中…

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