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Ammonium Chloride → 4-{4-[(4-methylpiperazin-1-yl)methyl]tetrahydro-2H-pyran-4-yl}phenol

HRID 273003
ノート
印刷プレビュー

反応式

HRID 273003 の反応式
C[S-].[Na+].C[O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2([CH2:18][N:19]3[CH2:24][CH2:23][N:22]([CH3:25])[CH2:21][CH2:20]3)[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)=[CH:8][CH:7]=1.[Cl-].[NH4+]>CN(C)C=O>[CH3:25][N:22]1[CH2:21][CH2:20][N:19]([CH2:18][C:12]2([C:9]3[CH:8]=[CH:7][C:6]([OH:5])=[CH:11][CH:10]=3)[CH2:13][CH2:14][O:15][CH2:16][CH2:17]2)[CH2:24][CH2:23]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 25517Ammonium ChlorideHCID 4378561Sodium methanethiolateHCID 685756701-{[4-(4-methoxyphenyl)tetrahydro-2H-pyran-4-yl]methyl}4-methylpiperazine

生成物 1

HCID 685768084-{4-[(4-methylpiperazin-1-yl)methyl]tetrahydro-2H-pyran-4-yl}phenol収率 103.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

反応条件

温度
130 °C

実験手順

To a suspension of sodium thiomethoxide (660 mg, 9.4 mmol) in N,N-dimethylformamide (2 ml) was added 1-{[4-(4-methoxyphenyl)tetrahydro-2H-pyran-4-yl]methyl}4-methylpiperazine (410 mg, 1.3 mmol) in N,N-dimethylformamide (3 ml). The reaction mixture was heated to 130° C. under nitrogen for 18 hours. The mixture was then allowed to cool down to room temperature and saturated aqueous ammonium chloride was added. The mixture was extracted with ethyl acetate (2×30 ml). The combined organic extracts were dried over sodium sulphate, filtered and concentrated in vacuo to provide a pale brown oil. This was azeotroped with toluene and dried under high vacuum to provide the title compound (390 mg, 100%) as an off-white solid. HRMS ESI+ m/z 291.2062 [MH]+.

後処理

  1. temperatureto cool down to room temperature
  2. extractionThe mixture was extracted with ethyl acetate (2×30 ml)
  3. dry with materialThe combined organic extracts were dried over sodium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto provide a pale brown oil
  7. customThis was azeotroped with toluene
  8. customdried under high vacuum

出典と根拠

ORDレコード
ord-5a2bdd95eef6439992dd03c805fd6110
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07456164B2

反応ノート

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