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Benzoic Acid → HCID 60962724、化合物

HRID 2380971
ノート
印刷プレビュー

反応式

HRID 2380971 の反応式
[C:1]([OH:9])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[C:11]1([CH:17]2[O:22][CH2:21][CH2:20][NH:19][CH2:18]2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C([N:25](CC)CC)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>C(#N)C.ClCCl>[NH2:25][C:5]1[CH:6]=[CH:7][C:2]([C:1]([N:19]2[CH2:20][CH2:21][O:22][CH:17]([C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH2:18]2)=[O:9])=[CH:3][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 243Benzoic AcidHCID 8471TriethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 123435392-Phenylmorpholine hydrochloride

生成物 1

HCID 60962724HCID 60962724、化合物収率 85%

試薬・触媒・溶媒 2

HCID 6342
Acetonitrile
溶媒
HCID 6344Dichloromethane溶媒

実験手順

To a stirred suspension of benzoic acid (160 mg, 1 mmol) and 2-phenylmorpholine hydrochloride (300 mg, 1.5 mmol) in acetonitrile (10 ml) was added triethylamine (0.4 ml, 3 mmol) followed by HATU and the reaction mixture was stirred at room temperature for 16 hours. The reaction was diluted with dichloromethane (25 ml) and washed with sodium hydrogen carbonate (25 ml, saturated solution). The organics were collected, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel, eluting with ethylacetate to afford the title compound as a clear oil (240 mg, 84% yield). HPLC retention time 5.05 min. Mass spectrum (ES+) m/z 283 (M+H).

後処理

  1. washwashed with sodium hydrogen carbonate (25 ml, saturated solution)
  2. customThe organics were collected
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by flash chromatography on silica gel
  6. washeluting with ethylacetate

出典と根拠

ORDレコード
ord-dda36f40f4ba44969869b63ef25201cf
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08258138B2

反応ノート

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