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Dimethylformamide → 5-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)pyridine-2-carboxamide

HRID 341431
ノート
印刷プレビュー

反応式

HRID 341431 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([N:8]([CH3:15])[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:5]=[C:4]([C:16]2[N:20]=[C:19]([C:21]3[CH:22]=[CH:23][C:24]([C:27](O)=[O:28])=[N:25][CH:26]=3)[O:18][N:17]=2)[N:3]=1.C(Cl)(=O)C(Cl)=O.C[N:37](C=O)C>ClCCCl.CO>[NH2:1][C:2]1[N:7]=[C:6]([N:8]([CH3:15])[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:5]=[C:4]([C:16]2[N:20]=[C:19]([C:21]3[CH:22]=[CH:23][C:24]([C:27]([NH2:37])=[O:28])=[N:25][CH:26]=3)[O:18][N:17]=2)[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 668034705-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)pyridine-2-carboxylic acid2 回

生成物 1

HCID 668030815-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)pyridine-2-carboxamide収率 30%

試薬・触媒・溶媒 2

HCID 11
1,2-Dichloroethane
溶媒
HCID 887Methanol溶媒

実験手順

To a solution of 5-(3-{4-amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)pyridine-2-carboxylic acid (Intermediate 124, 50 mg, 128 μmol) in DCE (10 mL) and DMF (100 μL) was added oxalyl chloride (22 μL, 256 μmol). The resulting solution was stirred at room temperature for 2 h, evaporated to dryness and re-suspended in a solution of ammonia in dioxane (7N, 10 mL). The reaction mixture was stirred overnight at room temperature and then poured into water (50 mL). The mixture was extracted with DCM (3×50 mL) and the combined organics were dried and concentrated under vacuum to afford a crude yellow solid. The crude material was suspended in MeOH, filtered and washed with further MeOH. The resulting solid was recrystallised in dioxane and water to afford the title compound as a white solid (15 mg, 30%).

後処理

  1. customevaporated to dryness
  2. stirringThe reaction mixture was stirred overnight at room temperature
  3. additionpoured into water (50 mL)
  4. extractionThe mixture was extracted with DCM (3×50 mL)
  5. customthe combined organics were dried
  6. concentrationconcentrated under vacuum
  7. customto afford a crude yellow solid
  8. filtrationfiltered
  9. washwashed with further MeOH
  10. customThe resulting solid was recrystallised in dioxane

出典と根拠

ORDレコード
ord-ccf8fc889d774f8b9705f79f65b1f591
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895733B2

反応ノート

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