Sodium Bicarbonate → (E)-N-(4-amino-5-(quinolin-3-yl)-6,7,8,9-tetrahydropyrimido[5,4-b]indolizin-8-yl)-4-(dimethylamino)-2-butenamide

HRID 336146ノート

反応式

HRID 336146 の反応式
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[N:25]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=[C:27]([C:35]2[C:36]3[C:48]([NH2:49])=[N:47][CH:46]=[N:45][C:37]=3[N:38]3[C:43]=2[CH2:42][CH2:41][CH:40]([NH2:44])[CH2:39]3)[CH:26]=1.Cl.[CH3:51][N:52]([CH3:59])[CH2:53]/[CH:54]=[CH:55]/[C:56](O)=[O:57].C(=O)(O)[O-].[Na+]>CN(C=O)C>[NH2:49][C:48]1[C:36]2[C:35]([C:27]3[CH:26]=[N:25][C:34]4[C:29]([CH:28]=3)=[CH:30][CH:31]=[CH:32][CH:33]=4)=[C:43]3[N:38]([C:37]=2[N:45]=[CH:46][N:47]=1)[CH2:39][CH:40]([NH:44][C:56](=[O:57])/[CH:55]=[CH:54]/[CH2:53][N:52]([CH3:59])[CH3:51])[CH2:41][CH2:42]3

参加物

6

反応物 4

HCID 516892Sodium BicarbonateHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 45358758(2E)-4-(Dimethylamino)-2-butenoic acid hydrochlorideHCID 867112835-(Quinolin-3-yl)-6,7,8,9-tetrahydropyrimido[5,4-b]indolizine-4,8-diamine

生成物 1

HCID 71721577(E)-N-(4-amino-5-(quinolin-3-yl)-6,7,8,9-tetrahydropyrimido[5,4-b]indolizin-8-yl)-4-(dimethylamino)-2-butenamide収率 54.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

HATU (10.3 mg) and 5-(quinolin-3-yl)-6,7,8,9-tetrahydropyrimido[5,4-b]indolizine-4,8-diamine (8.8 mg) obtained in Step 11 of Example 1 were added to a solution of trans-4-dimethylaminocrotonic acid hydrochloride (4.5 mg) in DMF (0.5 ml) at room temperature. After being stirred for 1 hour at the same temperature, the mixture was poured into a saturated aqueous sodium bicarbonate solution, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was then distilled off under reduced pressure. The resulting residue was purified by preparative thin-layer chromatography (produced by Wako, NH2 silica-gel 60 F254 plate, developing solvent: chloroform/methanol) to obtain the title compound as a light-yellow solid (6.4 mg).

後処理

  1. extractionfollowed by extraction with ethyl acetate
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. distillationthe solvent was then distilled off under reduced pressure
  4. customThe resulting residue was purified by preparative thin-layer chromatography (produced by Wako, NH2 silica-gel 60 F254 plate, developing solvent: chloroform/methanol)

出典と根拠

ORDレコード
ord-9d74c321996546108d8d7e0fe803c386
出典データセット
uspto-grants-2014_11
特許番号
US08889666B2

反応ノート

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