Dimethylformamide → 4-methoxy-3-[2-(1-pyrrolidinyl)ethoxy]Benzenamine

HRID 2420706ノート

反応式

HRID 2420706 の反応式
CN(C=O)C.[CH3:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[CH:10][C:9]=1[OH:17].Cl.Cl[CH2:20][CH2:21][N:22]1[CH2:26][CH2:25][CH2:24][CH2:23]1.C([O-])([O-])=O.[K+].[K+]>O>[CH3:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][C:9]=1[O:17][CH2:20][CH2:21][N:22]1[CH2:26][CH2:25][CH2:24][CH2:23]1

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 694712-Methoxy-5-nitrophenolHCID 816681-(2-Chloroethyl)pyrrolidine hydrochloride

生成物 1

HCID 189801284-methoxy-3-[2-(1-pyrrolidinyl)ethoxy]Benzenamine収率 87%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A stirred DMF suspension (5 mL) of 2-methoxy-5-nitrophenol (0.5 g, 2.96 mmol), 1-(2-chloroethyl)pyrrolidine hydrochloride (0.75 g (4.43 mmol) and K2CO3 (1.02 g, 7.4 mmol) was heated at 80° C. for 2 hr. After cooling to RT, the reaction was diluted with 20 mL of H2O and extracted with EtOAc (3×20 mL). The combined EtOAc layers were washed brine and dried over MgSO4. After concentration under vacuum, the resulting residue was chromatographed on silica gel. Gradient elution CH2Cl2 to 10% MeOH/CH2Cl2 eluted N-(2-(2-methoxy-5-nitrophenoxy)ethyl)pyrrolidine (507 mg) as a light orange solid. Subsequent conversion of the aryl nitro substituent to the title aryl amine was accomplished in 87% yield following the procedure described in step C of Example 6. MS (ESI) 237 (M+H)+.

後処理

  1. extractionextracted with EtOAc (3×20 mL)
  2. washThe combined EtOAc layers were washed brine
  3. dry with materialdried over MgSO4
  4. concentrationAfter concentration under vacuum
  5. customthe resulting residue was chromatographed on silica gel
  6. washGradient elution CH2Cl2 to 10% MeOH/CH2Cl2
  7. washeluted N-(2-(2-methoxy-5-nitrophenoxy)ethyl)pyrrolidine (507 mg) as a light orange solid

出典と根拠

ORDレコード
ord-ff570ea0fd524669a1dbba79be46385a
出典データセット
uspto-grants-2011_06
特許番号
US07956049B2

反応ノート

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