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Triethylamine → HCID 59837478、化合物

HRID 272964
ノート
印刷プレビュー

反応式

HRID 272964 の反応式
CN(C(ON1N=NC2C1=CC=CC=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH:25]([N:28]1[CH2:33][CH2:32][CH:31]([O:34][C:35]2[CH:40]=[CH:39][C:38]([C:41]3([C:47]([OH:49])=O)[CH2:46][CH2:45][O:44][CH2:43][CH2:42]3)=[CH:37][CH:36]=2)[CH2:30][CH2:29]1)([CH3:27])[CH3:26].[CH2:50]([N:52](CC)[CH2:53]C)[CH3:51].C(NC)C>CN(C)C=O>[CH2:50]([N:52]([CH3:53])[C:47]([C:41]1([C:38]2[CH:39]=[CH:40][C:35]([O:34][CH:31]3[CH2:32][CH2:33][N:28]([CH:25]([CH3:26])[CH3:27])[CH2:29][CH2:30]3)=[CH:36][CH:37]=2)[CH2:42][CH2:43][O:44][CH2:45][CH2:46]1)=[O:49])[CH3:51]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 12219N-MethylethylamineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 598374534-{4-[(1-Isopropylpiperidin-4-yl)oxy]phenyl}tetrahydro-2H-pyran-4-carboxylic acid

生成物 1

HCID 59837478HCID 59837478、化合物収率 35.5%

試薬・触媒・溶媒

1
HCID 6228Dimethylformamide溶媒

実験手順

O-(1H-Benzotriazol-1-yl)-N,N,N′N′-tetramethyluronium hexafluorophosphate (286 mg, 0.75 mmol) was added to a solution of 4-{4-[(1-isopropylpiperidin-4-yl)oxy]phenyl}tetrahydro-2H-pyran-4-carboxylic acid (200 mg, 0.58 mmol) in N,N-dimethylformamide (6 mL). Then triethylamine (243 μL, 1.74 mmol) was added. The mixture was stirred at room temperature for 15 minutes. Ethylmethylamine (500 μL, 5.8 mmol) was added and the reaction mixture stirred at room temperature for 18 hours. The reaction was concentrated in vacuo. The residue was partitioned between aqueous sodium bicarbonate solution (30 mL) and ethyl acetate (2×75 mL). The organics were combined, dried over sodium sulphate, filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography on silica gel eluting with dichloromethane:methanol:ammonia (96:4:0.5, by volume) to provide the title compound (80 mg, 35%). 1H NMR (400 MHz, CD3OD) δ 1.06-1.25 (m, 9H), 1.90-2.02 (m, 4H), 2.08-2.12 (m, 2H), 2.25-2.28 (m, 2H), 2.58 (m, 2H), 2.87 (m, 3H), 2.95 (m, 2H), 3.09-3.12 (m, 3H), 3.71-3.76 (m, 2H), 3.82-3.86 (m, 2H), 4.53 (m, 1H), 6.98 (d, 2H), 7.20 (d, 2H).

後処理

  1. stirringthe reaction mixture stirred at room temperature for 18 hours
  2. concentrationThe reaction was concentrated in vacuo
  3. customThe residue was partitioned between aqueous sodium bicarbonate solution (30 mL) and ethyl acetate (2×75 mL)
  4. dry with materialdried over sodium sulphate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe crude product was purified by flash chromatography on silica gel eluting with dichloromethane:methanol:ammonia (96:4:0.5, by volume)

出典と根拠

ORDレコード
ord-5172bda429c84ec0868dc752792a5b5d
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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