Acetic Acid → HCID 86722609、化合物

HRID 2271498ノート

反応式

HRID 2271498 の反応式
[CH2:1]([N:3]([CH2:6][CH3:7])[CH2:4]C)C.Cl.[Cl:9][C:10]1[CH:11]=[C:12]([CH:17]([O:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)C2CNC2)[CH:13]=[CH:14][C:15]=1[Cl:16].C=O.C(O)(=O)C.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+].[OH-].[Na+]>CO>[Cl:9][C:10]1[CH:11]=[C:12]([CH:17]([O:22][C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH:7]2[CH2:4][N:3]([CH3:1])[CH2:6]2)[CH:13]=[CH:14][C:15]=1[Cl:16]

参加物

8

実験手順

Triethylamine (0.2 mL, 1.313 mmol) was added to 20 mL of 3-((3,4-dichlorophenyl)(phenoxy)methyl)azetidine hydrochloride (300 mg, 0.870 mmol) dissolved in a methanol solution, and the mixture was stirred at room temperature for 1 hour. 37% formaldehyde aqueous solution (0.3 ml, 3.50 mmol) and acetic acid (0.2 ml, 3.50 mmol) were added to the reaction mixture, and NaBH(OAc)3 (742 mg, 3.50 mmol) was added thereto, followed by stirring for one day. Thereafter, 1 mL of 1 N NaOH was added thereto, and the mixture was stirred for 30 minutes. The organic layer was washed with distilled water, and the organic layer was adjusted to pH 7 using a 1 N NaOH aqueous solution, and extracted with methylene chloride (3*30 mL) and dried over anhydrous magnesium sulfate. The solvent was removed by reduced pressure evaporation to obtain a colorless liquid, which was purified by flash chromatography (methylene chloride:methanol (9:1, v/v)). The product was identified as a single compound by TLC (methylene chloride:methanol (9:1, v/v)).

後処理

  1. additionwas added
  2. stirringby stirring for one day
  3. stirringthe mixture was stirred for 30 minutes
  4. washThe organic layer was washed with distilled water
  5. extractionextracted with methylene chloride (3*30 mL)
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe solvent was removed by reduced pressure evaporation
  8. customto obtain a colorless liquid, which
  9. customwas purified by flash chromatography (methylene chloride:methanol (9:1

出典と根拠

ORDレコード
ord-b7f84c681cae46b08c1c88296b9dc7f3
出典データセット
uspto-grants-2015_09
特許番号
US09120771B2

反応ノート

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