Sodium Nitrite → (6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl-1H-[1,2,3]triazolo[4,5-c]pyridine

HRID 1511273ノート

反応式

HRID 1511273 の反応式
[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[N:11]([C:13]([CH2:16][NH:17][C:18]4[CH:23]=[CH:22][N:21]=[CH:20][C:19]=4[NH2:24])=[N:14][N:15]=3)[N:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:25]([O-])=O.[Na+]>CC(O)=O.O>[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[N:11]([C:13]([CH2:16][N:17]4[C:18]5[CH:23]=[CH:22][N:21]=[CH:20][C:19]=5[N:24]=[N:25]4)=[N:14][N:15]=3)[N:12]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

参加物

5

実験手順

To a solution of N4-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)pyridine-3,4-diamine (0.0640 g, 0.202 mmol) in HOAc (5 mL) was added sodium nitrite (0.0153 g, 0.222 mmol) in water (2 mL). Stirred for 1 h. Concentrated. Took up in DMSO and purified on RPHPLC. Took fractions containing product and made basic with 91 sodium carbonate and removed volatiles in vacuo. Product crashed out and was isolated by filtration. MS m/z=329.2[M+1]+. Calc'd for C17H12N8: 328.3.

後処理

  1. concentrationConcentrated
  2. custompurified on RPHPLC
  3. additionTook fractions containing product
  4. customremoved volatiles in vacuo
  5. customwas isolated by filtration

出典と根拠

ORDレコード
ord-e0fa9c7c04de480db4ea259fa3106b61
出典データセット
uspto-grants-2012_07
特許番号
US08212041B2

反応ノート

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