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Dimethylformamide → 4-(1-(2,4-dimethyl-5-(6-(pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-2-yl)benzoyl)piperidin-4-yl)benzonitrile

HRID 541202
ノート
印刷プレビュー

反応式

HRID 541202 の反応式
[N:1]1([C:6]2[N:11]=[CH:10][C:9]([NH2:12])=[C:8]([NH2:13])[CH:7]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:14]([C:16]1[C:17]([CH3:39])=[CH:18][C:19]([CH3:38])=[C:20]([CH:37]=1)[C:21]([N:23]1[CH2:28][CH2:27][CH:26]([C:29]2[CH:36]=[CH:35][C:32]([C:33]#[N:34])=[CH:31][CH:30]=2)[CH2:25][CH2:24]1)=[O:22])=O.S(S([O-])=O)([O-])(=O)=O.[Na+].[Na+].CN(C=O)C>O>[CH3:38][C:19]1[CH:18]=[C:17]([CH3:39])[C:16]([C:14]2[NH:12][C:9]3[CH:10]=[N:11][C:6]([N:1]4[CH2:5][CH2:4][CH2:3][CH2:2]4)=[CH:7][C:8]=3[N:13]=2)=[CH:37][C:20]=1[C:21]([N:23]1[CH2:24][CH2:25][CH:26]([C:29]2[CH:36]=[CH:35][C:32]([C:33]#[N:34])=[CH:31][CH:30]=2)[CH2:27][CH2:28]1)=[O:22]
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

6

反応物 4

HCID 6228DimethylformamideHCID 656671Sodium PyrosulfiteHCID 682882956-(Pyrrolidin-1-YL)pyridine-3,4-diamine2 回HCID 866725224-(1-(5-Formyl-2,4-dimethylbenzoyl)piperidin-4-yl)benzonitrile2 回

生成物 1

HCID 682883844-(1-(2,4-dimethyl-5-(6-(pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-2-yl)benzoyl)piperidin-4-yl)benzonitrile収率 13.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

To a 100 mL round bottom flask was added 6-(pyrrolidin-1-yl)pyridine-3,4-diamine (compound 20.2, 641 mg, 3.60 mmol, 1.0 equiv), 4-(1-(5-formyl-2,4-dimethylbenzoyl)piperidin-4-yl)benzonitrile (compound 16.4, 1.25 g, 3.60 mmol, 1.0 equiv), sodium metabisulfite (890 mg, 4.68 mmol, 1.3 equiv) and DMF (36 mL). The mixture was heated at 100° C. under air for 22 hours then allowed to cool to room temperature. Water (80 mL) was added slowly to the stirred solution until no further product precipitated. The solids were filtered and washed with water (2×15 mL) and dried to a brown solid (1.42 g). Additional product precipitated from the filtrate upon standing which was filtered and washed with water (2×10 mL) to obtain an off white solid (241 mg). The above reaction was repeated a second time in the exact manner and quantities as described to yield additional product (1.26 g of brown solid upon initial precipitation, plus 288 mg of off white solid from additional precipitation). The aqueous filtrates from the two reactions were combined and aqueous NaHCO3 was added to adjust the pH to 7. The aqueous was extracted with DCM/2% MeOH (300 mL), dried (Na2SO4), filtered and evaporated to obtain a brown solid (547 mg). All products obtained were combined and purified by silica gel chromatography (DCM/MeOH) to obtain the title compound as a yellow solid (2.37 g, 65% based on the theoretical yield for the two reactions). m/z (ES+) 505.1 (M+H)+. 1H NMR (400 MHz, DMSO-d6): δ 12.41 (br s, 1H), 8.52 (s, 1H), 7.77 (d, J=8.2 Hz, 2H), 7.66 & 7.56 (2 br singlets, amide rotamers, ArH, 1H), 7.49 (s, J=8.2 Hz, 2H), 7.29 (s, 1H), 6.31 (br s, 1H), 4.79-4.67 (m, 1H), 3.54-3.34 (m, 5H), 3.17 (app t, J=11.8, 1H), 2.99-2.82 (m, 2H), 2.63 (s, 3H), 2.33 & 2.24 (2 singlets, amide rotamers, ArCH3, 3H), 2.03-1.87 (m, 5H), 1.82-1.38 (m, 3H). Elemental analysis (C31H32N6O.1.3H2O, 528.04), found (calcd), C, 70.66 (70.51); H, 6.54 (6.60); N, 15.78 (15.92).

後処理

  1. temperatureto cool to room temperature
  2. customprecipitated
  3. filtrationThe solids were filtered
  4. washwashed with water (2×15 mL)
  5. dry with materialdried to a brown solid (1.42 g)
  6. customAdditional product precipitated from the filtrate
  7. filtrationwas filtered
  8. washwashed with water (2×10 mL)

出典と根拠

ORDレコード
ord-408a29e931974850bbe10cef0b45aac1
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871790B2

反応ノート

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