Glycolic Acid → (6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanol

HRID 40178

反応式

HRID 40178 の反応式
[C:1]1([C:7]2[N:12]=[N:11][C:10]([NH:13][NH2:14])=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:15](O)(=O)[CH2:16][OH:17].CC1C=CC(S(O)(=O)=O)=CC=1.O>C1(C)C=CC=CC=1>[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[N:11]([C:15]([CH2:16][OH:17])=[N:14][N:13]=3)[N:12]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

参加物

5

反応物 3

HCID 757Glycolic AcidHCID 521998p-Toluenesulfonic acid monohydrateHCID 64098423-Hydrazinyl-6-phenylpyridazine

生成物 1

HCID 57812703(6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanol

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A mixture of 1-(6-phenylpyridazin-3-yl)hydrazine (2.00 g, 10.7 mmol), glycolic acid (0.825 g, 10.8 mmol), p-TsOH.H2O (2.55 g, 13.4 mmol) in PhMe (50 mL) was refluxed for 14 h. PhMe was removed in vacuo. The resulting solids were diluted with water (30 mL). The mixture was brought to pH˜10 with 2N NaOH. The solids were isolated solid by filtration, washed with water and dried under vacuum to give an off white solid which was used without further purification. (ESI, pos. ion) m/z: 227.0 (M+H).

後処理

  1. temperaturewas refluxed for 14 h
  2. customPhMe was removed in vacuo
  3. additionThe resulting solids were diluted with water (30 mL)
  4. customThe solids were isolated solid
  5. filtrationby filtration
  6. washwashed with water
  7. customdried under vacuum
  8. customto give an off white solid which
  9. customwas used without further purification

出典と根拠

ORDレコード
ord-6989f4bd20934af588a402f67981da7d
出典データセット
uspto-grants-2013_09
特許番号
US08524900B2

関連ノート

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