Acetic Acid → 2-[5-(4-Azepan-1-yl-piperidin-1-yl)-2-chloro-phenyl]-1H-benzoimidazole

HRID 2047382

反応式

HRID 2047382 の反応式
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:11]=[C:12]([N:17]2[CH2:22][CH2:21][C:20](=O)[CH2:19][CH2:18]2)[CH:13]=[CH:14][C:15]=1[Cl:16].[NH:24]1[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[N:24]1([CH:20]2[CH2:21][CH2:22][N:17]([C:12]3[CH:13]=[CH:14][C:15]([Cl:16])=[C:10]([C:2]4[NH:3][C:4]5[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=5[N:1]=4)[CH:11]=3)[CH2:18][CH2:19]2)[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1

参加物

6

反応物 4

HCID 176Acetic AcidHCID 8119Azepane2 回HCID 5049666Sodium triacetoxyborohydrideHCID 595682431-[3-(1H-benzo[d]imidazol-2-yl)-4-chlorophenyl]piperidin-4-one

生成物 1

HCID 441241202-[5-(4-Azepan-1-yl-piperidin-1-yl)-2-chloro-phenyl]-1H-benzoimidazole収率 58%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a suspension of 1-[3-(1H-benzoimidazol-2-yl)-4-chloro-phenyl]-piperidin-4-one (0.10 g, 0.31 mmol) in dichloromethane (2 mL) was added azepane (0.05 mL, 0.46 mmol). After 30 min stirring at room temperature a drop of acetic acid was added, and after 1 h a further aliquot of azepane (0.05 mL, 0.46 mmol) was added, followed by sodium triacetoxyborohydride (NaB(OAc)3H) (0.10 g, 0.46 mmol). The reaction mixture was stirred at room temperature overnight, then the solvent was removed under reduced pressure, and the crude product dissolved in dichloromethane (10 mL). To the solution PS-isocyanate resin (PS-NCO) (Argonaut, loading 0.93 mmol/g) was added, then the mixture was shaken at room temperature overnight and filtered. The solvent was removed under reduced pressure to obtain a solid residue that was washed with EtOAc and Et2O then dried to give the desired product (0.07 g, 58%).

後処理

  1. additionwas added
  2. customthe solvent was removed under reduced pressure
  3. dissolutionthe crude product dissolved in dichloromethane (10 mL)
  4. additionTo the solution PS-isocyanate resin (PS-NCO) (Argonaut, loading 0.93 mmol/g) was added
  5. stirringthe mixture was shaken at room temperature overnight
  6. filtrationfiltered
  7. customThe solvent was removed under reduced pressure
  8. customto obtain a solid residue that
  9. washwas washed with EtOAc and Et2O
  10. customthen dried

出典と根拠

ORDレコード
ord-c92a700be4a84b15b19ba1d6ccec95b2
出典データセット
uspto-grants-2013_11
特許番号
US08592463B2

関連ノート

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