Water → HCID 67050039、化合物

HRID 2063321ノート

反応式

HRID 2063321 の反応式
CN(C(ON1N=N[C:11]2[CH:12]=[CH:13][CH:14]=[N:15][C:10]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[NH2:25][C:26]1[C:30]([NH:31][C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])=[CH:29][S:28][CH:27]=1.CN1C[CH2:44][O:43][CH2:42]C1.[OH2:46].CN([CH:50]=[O:51])C>C(OCC)(=O)C>[C:35]([O:34][C:32]([NH:31][C:30]1[C:26]([NH:25][C:50]([C:10]2[CH:11]=[CH:12][C:13]([C:42]([O:43][CH3:44])=[O:46])=[CH:14][N:15]=2)=[O:51])=[CH:27][S:28][CH:29]=1)=[O:33])([CH3:38])([CH3:37])[CH3:36]

参加物

7

実験手順

HATU (1.3 g, 3.5 mmol) was added to a solution of 3-amino-4-t-butoxycarbonylaminothiophene (Reference Compound No. 1-1, 0.68 g, 3.2 mmol), 5-methexycarbonylpyridine-2-carboxylic acid (0.64 g, 3.5 mmol), and N-methylmorpholine (0.70 mL, 6.4 mmol) in DMF (20 mL), and then the reaction mixture was stirred at room temperature overnight. Water (0.30 L) and ethyl acetate (0.40 L) were added thereto, and the insoluble materials were filtered off to give 0.50 g of the title reference compound as a pale yellow solid. The filtrate was partitioned and the organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and then the obtained solid was collected by filtration with ethylacetate (30 mL) to give 0.30 g of the title reference compound as a pale brown solid. (Yield 67%)

後処理

  1. filtrationthe insoluble materials were filtered off
  2. customto give 0.50 g of the title reference compound as a pale yellow solid
  3. customThe filtrate was partitioned
  4. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. filtrationthe obtained solid was collected by filtration with ethylacetate (30 mL)
  7. customto give 0.30 g of the title reference compound as a pale brown solid

出典と根拠

ORDレコード
ord-0bf37e2b520e4fb484146e4d02b9c588
出典データセット
uspto-grants-2012_10
特許番号
US08288380B2

反応ノート

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