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Methanol → 7-(4-((4-Chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylic acid

HRID 1021370
ノート
印刷プレビュー

反応式

HRID 1021370 の反応式
[Cl:1][C:2]1[CH:37]=[CH:36][C:5]([CH2:6][CH2:7][NH:8][C:9]([C:11]2[CH:35]=[CH:34][C:14]([O:15][C:16]3[CH:25]=[C:24]4[C:19]([CH:20]([C:28]([O:30]C)=[O:29])[CH2:21][C:22]([CH3:27])([CH3:26])[O:23]4)=[CH:18][C:17]=3[C:32]#[N:33])=[CH:13][CH:12]=2)=[O:10])=[CH:4][CH:3]=1.[OH-].[Na+].O.CO>C1COCC1.C(OCC)(=O)C.Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][CH2:7][NH:8][C:9]([C:11]2[CH:12]=[CH:13][C:14]([O:15][C:16]3[CH:25]=[C:24]4[C:19]([CH:20]([C:28]([OH:30])=[O:29])[CH2:21][C:22]([CH3:26])([CH3:27])[O:23]4)=[CH:18][C:17]=3[C:32]#[N:33])=[CH:34][CH:35]=2)=[O:10])=[CH:36][CH:37]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 887MethanolHCID 962WaterHCID 14798Sodium HydroxideHCID 67080218Methyl 7-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylate

生成物 1

HCID 670804237-(4-((4-Chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylic acid収率 30.9%

試薬・触媒・溶媒 3

HCID 313
Hydrochloric Acid
溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

Methyl 7-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylate (2.0 mg, 0.00385 mmol) was diluted with THF (500 μL) followed by the addition of NaOH (0.00771 mL, 0.0385 mmol) and 200 μL of water and methanol. After stirring for 3 hours, the reaction was diluted with ethyl acetate and 2N HCl. The layers were separated and the organic layer was dried over MgSO4, filtered and concentrated. The material was purified using a 0.5 mm preparative TLC plate, eluting with 5% methanol/0.5% acetic acid/CH2Cl2 to yield the title compound (0.6 mg, 30.8% yield) as a white solid. MS (ESI)=504.9 (M+1).

後処理

  1. customThe layers were separated
  2. dry with materialthe organic layer was dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe material was purified
  6. washeluting with 5% methanol/0.5% acetic acid/CH2Cl2

出典と根拠

ORDレコード
ord-3598b875ce0940c584a5e054f5e89b78
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08716498B2

反応ノート

読み込み中…

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