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Sodium Chloride → N-((6-amino-2-methylpyridin-3-yl)methyl)-1-((2-methylquinolin-6-yl)methyl)-1H-pyrazole-4-carboxamide

HRID 928442
ノート
印刷プレビュー

反応式

HRID 928442 の反応式
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH2:12][N:13]3[CH:17]=[C:16]([C:18]([OH:20])=O)[CH:15]=[N:14]3)[CH:8]=2)[N:3]=1.[Na+].[Cl-].CCN=C=NCCCN(C)C.Cl.C1C=NC2N(O)N=NC=2C=1.CN1CCOCC1.[NH2:52][CH2:53][C:54]1[CH:55]=[CH:56][C:57]([NH2:61])=[N:58][C:59]=1[CH3:60]>CN(C=O)C.CO.C(#N)C>[NH2:61][C:57]1[N:58]=[C:59]([CH3:60])[C:54]([CH2:53][NH:52][C:18]([C:16]2[CH:15]=[N:14][N:13]([CH2:12][C:7]3[CH:8]=[C:9]4[C:4](=[CH:5][CH:6]=3)[N:3]=[C:2]([CH3:1])[CH:11]=[CH:10]4)[CH:17]=2)=[O:20])=[CH:55][CH:56]=1
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

10

反応物 6

HCID 5234Sodium ChlorideHCID 79724-MethylmorpholineHCID 181649HOAtHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 101977255-(Aminomethyl)-6-methylpyridin-2-amineHCID 580812841-((2-methylquinolin-6-yl)methyl)-1H-pyrazole-4-carboxylic acid

生成物 1

HCID 66723582
N-((6-amino-2-methylpyridin-3-yl)methyl)-1-((2-methylquinolin-6-yl)methyl)-1H-pyrazole-4-carboxamide

試薬・触媒・溶媒 3

HCID 887Methanol溶媒2 回HCID 6228Dimethylformamide溶媒HCID 6342Acetonitrile溶媒

反応条件

温度
50 °C

実験手順

To a suspension of 1-((2-methylquinolin-6-yl)methyl)-1H-pyrazole-4-carboxylic acid (incl. NaCl) (100 mg, 0.337 mmol), EDC.HCl (84 mg, 0.438 mmol) and HOAt (59.6 mg, 0.438 mmol) in DMF (1 ml) was added N-methylmorpholine (0.185 ml, 1.684 mmol). The reaction mixture was stirred for 1 h at 50° C., then 5-(aminomethyl)-6-methylpyridin-2-amine (70.7 mg, 0.337 mmol) was added. Stirring continued at 50° C. for 18 h. Reaction mixture was diluted with methanol, then applied onto a PL-SO3H cartridge (500 mg/6 ml by VARIAN) to catch the desired amine product, washed the cartridge with DMF, DCM and MeOH to remove all impurities, then the product was released from the cartridge by washing with 2M NH3 in MeOH. The basic filtrate was evaporated to give the crude material, which was treated with 0.2 ml of MeOH and 1 ml of ACN in ultrasonic bath. The precipitate formed was filtered, washed with 1 ml of ACN and dried under high vacuum for 4 days to yield the title compound. HPLC (Method J) Rt=2.373 min, MS (Method V) [M+H]+=387.1.

後処理

  1. stirringStirring
  2. waitcontinued at 50° C. for 18 h
  3. customReaction mixture
  4. washwashed the cartridge with DMF, DCM and MeOH
  5. customto remove all impurities
  6. washby washing with 2M NH3 in MeOH
  7. customThe basic filtrate was evaporated
  8. customto give the crude material, which
  9. customThe precipitate formed
  10. filtrationwas filtered
  11. washwashed with 1 ml of ACN
  12. customdried under high vacuum for 4 days

出典と根拠

ORDレコード
ord-1eee77baa79a4995a82d67ed559d2e14
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09290485B2

反応ノート

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