Potassium Acetate → N-(5-(2-(cyanoimino)-1-(6-(2-cyanopropan-2-yl)pyridin-3-yl)-3-methyl-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)-3-(trifluoromethyl)pyridin-2-yl)-2-propylpentanamide

HRID 2174957ノート

反応式

HRID 2174957 の反応式
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:15]3[N:14]=[CH:13][C:12]4[N:18]([CH3:35])[C:19](=[N:32][C:33]#[N:34])[N:20]([C:21]5[CH:22]=[N:23][C:24]([C:27]([C:30]#[N:31])([CH3:29])[CH3:28])=[CH:25][CH:26]=5)[C:11]=4[C:10]=3[CH:9]=2)=[CH:4][C:3]=1[C:36]([F:39])([F:38])[F:37].[C:40]([O-:43])(=O)[CH3:41].[K+]>C(OC(=O)C(CCC)CCC)(=O)C(CCC)CCC.O>[C:33]([N:32]=[C:19]1[N:18]([CH3:35])[C:12]2[CH:13]=[N:14][C:15]3[CH:16]=[CH:17][C:8]([C:5]4[CH:4]=[C:3]([C:36]([F:38])([F:37])[F:39])[C:2]([NH:1][C:40](=[O:43])[CH:41]([CH2:6][CH2:5][CH3:8])[CH2:2][CH2:3][CH3:4])=[N:7][CH:6]=4)=[CH:9][C:10]=3[C:11]=2[N:20]1[C:21]1[CH:22]=[N:23][C:24]([C:27]([C:30]#[N:31])([CH3:28])[CH3:29])=[CH:25][CH:26]=1)#[N:34]

参加物

5

反応物 2

HCID 517044Potassium AcetateHCID 56947515Panulisib

生成物 1

HCID 56599242N-(5-(2-(cyanoimino)-1-(6-(2-cyanopropan-2-yl)pyridin-3-yl)-3-methyl-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)-3-(trifluoromethyl)pyridin-2-yl)-2-propylpentanamide

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 109236242-Propylpentanoyl 2-propylpentanoate溶媒

実験手順

N-(8-(6-amino-5-(trifluoromethyl)pyridin-3-yl)-1-(6-(2-cyanopropan-2-yl)pyridin-3-yl)-3-methyl-1H-imidazo[4,5-c]quinolin-2(3H)-ylidene)cyanamide (Example 5, 0.379 mmol) was stirred in valproic anhydride (5 mL). Potassium acetate (0.379 mmol) was added to it and the reaction was carried out at 110-115° C. for 2 h. The reaction mixture was cooled, diluted with water and extracted with ethyl acetate. Organic layer was concentrated, dried using anhydrous sodium sulfate and purified on silica gel column to obtain the title compound. 1H NMR (300 MHz, DMSO-d6): δ 10.21 (s, 1H), 9.32 (s, 1H), 9.08 (s, 1H), 8.63 (s, 1H), 8.44 (d, J=5.1 Hz, 1H), 8.28 (d, J=5.1 Hz, 1H), 8.18-8.15 (m, 1H), 8.01 (d, J=5.1 Hz, 1H), 7.06 (s, 1H), 3.94 (s, 3H), 1.77 (s, 3H), 1.56 (m, 2H), 1.35 (s, 6H), 1.23 (s, 1H), 0.91 (s, 6H); MS (m/z): 654.4 (M+1)+.

後処理

  1. temperatureThe reaction mixture was cooled
  2. extractionextracted with ethyl acetate
  3. concentrationOrganic layer was concentrated
  4. customdried
  5. custompurified on silica gel column

出典と根拠

ORDレコード
ord-d6e73ebda33042709195d40f67f49998
出典データセット
uspto-grants-2015_06
特許番号
US09062046B2

反応ノート

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