Diisopropylethylamine → 5-(2-(1,3-dioxolan-2-yl)ethyl)-2-phenyl-N-(2-(thiazolo[5,4-b]pyridin-2-yl)phenyl)thiazole-4-carboxamide

HRID 1799119

反応式

HRID 1799119 の反応式
C[NH3+].F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.F[P-](F)(F)(F)(F)F.[O:34]1[CH2:38][CH2:37][O:36][CH:35]1[CH2:39][CH2:40][C:41]1[S:45][C:44]([C:46]2[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=2)=[N:43][C:42]=1[C:52]([OH:54])=O.CCN(C(C)C)C(C)C.[N:64]1[C:72]2[C:67](=[N:68][CH:69]=[CH:70][CH:71]=2)[S:66][C:65]=1[C:73]1[CH:79]=[CH:78][CH:77]=[CH:76][C:74]=1[NH2:75].C([O-])(O)=O.[Na+]>CN(C=O)C>[O:36]1[CH2:37][CH2:38][O:34][CH:35]1[CH2:39][CH2:40][C:41]1[S:45][C:44]([C:46]2[CH:47]=[CH:48][CH:49]=[CH:50][CH:51]=2)=[N:43][C:42]=1[C:52]([NH:75][C:74]1[CH:76]=[CH:77][CH:78]=[CH:79][C:73]=1[C:65]1[S:66][C:67]2[C:72]([N:64]=1)=[CH:71][CH:70]=[CH:69][N:68]=2)=[O:54]

参加物

7

反応物 5

HCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 581014682-(Thiazolo[5,4-b]pyridin-2-yl)anilineHCID 585519085-(2-(1,3-Dioxolan-2-yl)ethyl)-2-phenylthiazole-4-carboxylic acidHCID 866211442-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate Methanaminium

生成物 1

HCID 585519015-(2-(1,3-dioxolan-2-yl)ethyl)-2-phenyl-N-(2-(thiazolo[5,4-b]pyridin-2-yl)phenyl)thiazole-4-carboxamide収率 66%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate methanaminium (HATU) (669 mg, 1.8 mmol) was added to a solution of 5-(2-(1,3-dioxolan-2-yl)ethyl)-2-phenylthiazole-4-carboxylic acid (504 mg, 1.7 mmol), DIPEA (613 μL, 3.5 mmol), and 2-(thiazolo[5,4-b]pyridin-2-yl)aniline b(250 mg, 1.1 mmol) in DMF (7 mL). The reaction mixture was stirred for 16 h, poured into sat aq NaHCO3 and extracted with EtOAc. The organic fractions were washed with brine, dried and concentrated. The crude product was crystallized from EtOH to give 5-(2-(1,3-dioxolan-2-yl)ethyl)-2-phenyl-N-(2-(thiazolo[5,4-b]pyridin-2-yl)phenyl)thiazole-4-carboxamide (372 mg, 66% yield).

後処理

  1. additionpoured
  2. extractionextracted with EtOAc
  3. washThe organic fractions were washed with brine
  4. customdried
  5. concentrationconcentrated
  6. customThe crude product was crystallized from EtOH

出典と根拠

ORDレコード
ord-daf8f2ab3a134fd9b0af9d92f9cc8dce
出典データセット
uspto-grants-2013_01
特許番号
US08343997B2

関連ノート

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