Hydrochloric Acid → HCID 178501122、化合物

HRID 538074

反応式

HRID 538074 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][CH:11]=O)([O-:3])=[O:2].Cl.[CH3:14][O:15][C:16]([C@H:18]1[CH2:23][CH2:22][C@H:21]([CH2:24][NH2:25])[CH2:20][CH2:19]1)=[O:17].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].Cl>C(Cl)Cl>[CH3:14][O:15][C:16]([C@H:18]1[CH2:23][CH2:22][C@H:21]([CH2:24][NH:25][CH2:11][CH2:10][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N+:1]([O-:3])=[O:2])[CH2:20][CH2:19]1)=[O:17]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 5049666Sodium triacetoxyborohydrideHCID 108447642-NitrobenzeneacetaldehydeHCID 178501119HCID 178501119、化合物

生成物 1

HCID 178501122HCID 178501122、化合物収率 27%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of (2-Nitro-phenyl)-acetaldehyde (1 g, 5.98 mmol), trans-4-Aminomethyl cyclohexanecarboxylic acid methyl ester hydrogen chloride salt (1.37 g, 6.58 mmol) and TEA (0.92 mL, 6.58 mmol) in dry DCM was stirred at room temperature for 2.5 h. Sodium triacetoxy borohydride (2.53 g, 11.96 mmol) was added and the mixture stirred at room temperature for 25 min. Then (2N) HCl was added until acidic pH and the aqueous layer extracted with DCM. The organic layer was washed with a saturated solution of NaHCO3 and dried over Na2SO4 anhydrous and then evaporated to afford crude product. Finally, the crude product was purified by flash chromatography on silica (ETP/EtOAc 9/1→0/1) to obtain the titled compound (0.51 g, yield: 27%).

後処理

  1. extractionthe aqueous layer extracted with DCM
  2. washThe organic layer was washed with a saturated solution of NaHCO3
  3. dry with materialdried over Na2SO4 anhydrous
  4. customevaporated
  5. customto afford crude product
  6. customFinally, the crude product was purified by flash chromatography on silica (ETP/EtOAc 9/1→0/1)

出典と根拠

ORDレコード
ord-46d4c2e571d7477b818f60875b53b2d1
出典データセット
uspto-grants-2014_10
特許番号
US08865704B2

関連ノート

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