Triethylamine → 1-((1R,2S)-2-(((3-(4-fluorophenyl)propyl)(methyl)amino)methyl)cyclohexyl)-3-(3-(1-methyl-1H-tetrazol-5-yl)phenyl)urea

HRID 1592328ノート

反応式

HRID 1592328 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][N:11]([CH2:13][C@@H:14]2[CH2:19][CH2:18][CH2:17][CH2:16][C@H:15]2[NH2:20])[CH3:12])=[CH:4][CH:3]=1.C(N(CC)CC)C.C1([O:34][C:35](=O)[NH:36][C:37]2[CH:42]=[CH:41][CH:40]=[C:39]([C:43]3[N:47]([CH3:48])[N:46]=[N:45][N:44]=3)[CH:38]=2)C=CC=CC=1>C(#N)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][CH2:10][N:11]([CH2:13][C@@H:14]2[CH2:19][CH2:18][CH2:17][CH2:16][C@H:15]2[NH:20][C:35]([NH:36][C:37]2[CH:42]=[CH:41][CH:40]=[C:39]([C:43]3[N:47]([CH3:48])[N:46]=[N:45][N:44]=3)[CH:38]=2)=[O:34])[CH3:12])=[CH:6][CH:7]=1

参加物

5

反応物 3

HCID 8471TriethylamineHCID 22252681phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamateHCID 69426356(1R,2S)-2-({[3-(4-fluorophenyl)-propyl]-methyl-amino}-methyl)-cyclohexylamine

生成物 1

HCID 112369501-((1R,2S)-2-(((3-(4-fluorophenyl)propyl)(methyl)amino)methyl)cyclohexyl)-3-(3-(1-methyl-1H-tetrazol-5-yl)phenyl)urea収率 60.4%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

A solution of (1R,2S)-2-({[3-(4-fluorophenyl)-propyl]-methyl-amino}-methyl)-cyclohexylamine (72 mg, 259 μmol) in acetonitrile (2 mL) was treated with triethylamine (72 μL, 517 μmol) and [3-(1-methyl-1H-tetrazol-5-yl)-phenyl]-carbamic acid phenyl ester (76 mg, 259 μmol). The mixture was stirred at room temperature for 15.5 hours and then was concentrated under vacuum. The residue was dissolved in ethyl acetate, and the solution was washed sequentially with 1.0 M aqueous sodium hydroxide, water and saturated aqueous sodium chloride. The organic phase was dried over sodium sulfate and concentrated under vacuum. The residue was purified by flash chromatography, eluting with 4% methanol in dichloromethane containing 0.4% aqueous ammonium hydroxide, to provide a white amorphous solid (75 mg, 60%).

後処理

  1. concentrationwas concentrated under vacuum
  2. dissolutionThe residue was dissolved in ethyl acetate
  3. washthe solution was washed sequentially with 1.0 M aqueous sodium hydroxide, water and saturated aqueous sodium chloride
  4. dry with materialThe organic phase was dried over sodium sulfate
  5. concentrationconcentrated under vacuum
  6. customThe residue was purified by flash chromatography
  7. washeluting with 4% methanol in dichloromethane containing 0.4% aqueous ammonium hydroxide

出典と根拠

ORDレコード
ord-690b5b8d2d114d08b29bf7cd0069351d
出典データセット
uspto-grants-2007_11
特許番号
US07291744B2

反応ノート

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