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1-Iodohexane → HCID 67401054、化合物

HRID 906640
ノート
印刷プレビュー

反応式

HRID 906640 の反応式
[OH:1][CH:2]1[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.CCN(C(C)C)[CH:11]([CH3:13])[CH3:12].ClC1C=[CH:22][C:21]([C:24]([NH:26][CH2:27][C:28]2[S:32][C:31]([S:33](Cl)(=[O:35])=[O:34])=[CH:30][CH:29]=2)=O)=CC=1.[H-].[Na+].I[CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45]>C(Cl)Cl.ClCCCl.CN(C=O)C.CCOC(C)=O>[CH2:13]([N:26]([CH2:24][CH:21]=[CH2:22])[CH2:27][C:28]1[S:32][C:31]([S:33]([N:5]2[CH2:6][CH2:7][CH:2]([O:1][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45])[CH2:3][CH2:4]2)(=[O:34])=[O:35])=[CH:30][CH:29]=1)[CH:11]=[CH2:12]
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

10

反応物 5

HCID 125271-IodohexaneHCID 24758Sodium hydrideHCID 79341Piperidin-4-olHCID 81531DiisopropylethylamineHCID 27357135-((4-Chlorobenzamido)methyl)thiophene-2-sulfonyl chloride

生成物 1

HCID 67401054HCID 67401054、化合物

試薬・触媒・溶媒 4

HCID 11
1,2-Dichloroethane
溶媒
HCID 6228Dimethylformamide溶媒
HCID 6344Dichloromethane溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
70 °C

実験手順

To a solution of 4-hydroxy-piperidine (190 mg, 1.88 mmol) and DIEA (0.87 mL, 5.13 mmol) in 10 mL CH2Cl2 was added a solution of 5-({[1-(4-Chloro-phenyl)-methanoyl]-amino}-methyl)-thiophene-2-sulfonyl chloride 1b (500 mg, 1.71 mmol) in hot DCE. The reaction mixture was stirred for 4 h. 100 mL EtOAc were added and excess of amines were removed by extraction with HCl (1N). The sulfonamide intermediate was used without any further purification, where 300 mg (0.84 mmol) were dissolved in dry DMF under Ar. NaH (60 mg, 50% in parafine oil, 1.01 mmol) were added as a solid. The colour of the reaction changed to orange. The reaction mixture was stirred for 15′ until no gas evolution was observed anymore. Iodohexane (356 mg, 1.68 mmol) dissolved in 1 mL DMF was added to the above solution and the reaction mixture was heated at 70° C. overnight. DMF was evaporated to dryness and the crude was taken up in CH2Cl2. The organic layer was washed twice with water, dried over MgSO4 and evaporated to dryness. The crude was purified on silica gel using cyclohexane/EtOAc 3:1 as eluent to obtain 210 mg (59%) of pure 326a as a colorless oil.

後処理

  1. customwere removed by extraction with HCl (1N)
  2. customThe sulfonamide intermediate was used without any further purification, where 300 mg (0.84 mmol)
  3. dissolutionwere dissolved in dry DMF under Ar
  4. stirringThe reaction mixture was stirred for 15′ until no gas evolution
  5. additionwas added to the above solution
  6. customDMF was evaporated to dryness
  7. washThe organic layer was washed twice with water
  8. dry with materialdried over MgSO4
  9. customevaporated to dryness
  10. customThe crude was purified on silica gel

出典と根拠

ORDレコード
ord-5f5d8992766e4071981ca8bd53312e04
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08012995B1

反応ノート

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