Dimethylformamide → HCID 58014984、化合物

HRID 1676527ノート

反応式

HRID 1676527 の反応式
Cl.Cl.[CH3:3][S:4]([CH2:7][CH2:8][CH2:9][N:10]1[CH2:15][CH2:14][CH:13]([NH2:16])[CH2:12][CH2:11]1)(=[O:6])=[O:5].N1([O:26][C:27](=O)[C:28]2[CH:33]=[CH:32][C:31]([NH2:34])=[C:30]([O:35][CH3:36])[CH:29]=2)C2C=CC=CC=2N=N1.CN(C)C=O.C(N(CC)CC)C>ClCCl>[NH2:34][C:31]1[CH:32]=[CH:33][C:28]([C:27]([NH:16][CH:13]2[CH2:14][CH2:15][N:10]([CH2:9][CH2:8][CH2:7][S:4]([CH3:3])(=[O:6])=[O:5])[CH2:11][CH2:12]2)=[O:26])=[CH:29][C:30]=1[O:35][CH3:36]

参加物

6

実験手順

To a mixture of 2.3 g of 1-(3-methanesulfonyl-propyl)-piperidin-4-ylamine dihydrochloride, 2.7 g (0.0095 mole) of 4-amino-3-methoxy-benzoic acid benzotriazol-1-yl ester and 15 mL of dimethylformamide was added 4.0 g (0.0395 mole) of triethylamine. The mixture was stirred at room temperature for 20 hours, then diluted with 150 mL of dichloromethane. The mixture was washed twice with 100 mL of sodium bicarbonate, once with 50 mL of water, once with 50 mL of brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with dichloromethane-methanol (gradient, 100:0-80:20) to give 2.0 g of 4-amino-N-[1-(3-methanesulfonyl-propyl)-piperidin-4-yl]-3-methoxy-benzamide.

後処理

  1. washThe mixture was washed twice with 100 mL of sodium bicarbonate, once with 50 mL of water, once with 50 mL of brine
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel chromatography
  6. washeluting with dichloromethane-methanol (gradient, 100:0-80:20)

出典と根拠

ORDレコード
ord-e7c1cfcc53fb43d08405f509ec108626
出典データセット
uspto-grants-2011_08
特許番号
US08003785B2

反応ノート

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