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Methanesulfonyl chloride → HCID 21993950、化合物

HRID 1978369
ノート
印刷プレビュー

反応式

HRID 1978369 の反応式
[C:1]([S:4][CH2:5][P:6]([O:11][CH2:12][CH3:13])([O:8][CH2:9][CH3:10])=[O:7])(=O)[CH3:2].C[O-].[Na+].CO.S(OCC1[CH2:30][CH2:29][N:28]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH2:27][CH2:26]1)(C)(=O)=O.CS(Cl)(=O)=O.OCSCC1CCN(C(OC(C)(C)C)=O)CC1>CO.O1CCCC1.O.C(N(CC)CC)C>[CH2:9]([O:8][P:6]([CH2:5][S:4][CH2:1][CH:2]1[CH2:30][CH2:29][N:28]([C:31]([O:33][C:34]([CH3:36])([CH3:35])[CH3:37])=[O:32])[CH2:27][CH2:26]1)([O:11][CH2:12][CH3:13])=[O:7])[CH3:10]
参加物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 31297Methanesulfonyl chlorideHCID 2765838Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 12536443S-[(Diethoxyphosphoryl)methyl] ethanethioateHCID 21993708HCID 21993708、化合物HCID 23694274Sodium methanolate methanol

生成物 1

HCID 21993950HCID 21993950、化合物

試薬・触媒・溶媒 4

HCID 887Methanol溶媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒HCID 8471Triethylamine溶媒

実験手順

To a solution of 1.529 g (6.759 mM) of S-(diethoxyphosphorylmethyl) thioacetate in 30 ml of methanol was added 1.30 g (6.76 mM) of 28% sodium methoxide-methanol under ice-cooling and the mixture was stirred at the prevailing temperature for 20 minutes. To this reaction mixture was added crude tert-butyl 4-(mesyloxymethyl)piperidine-1-carboxylate [which was prepared by adding 0.73 ml (9.46 mM) of methanesulfonyl chloride to a solution of 1.75 g (8.11 mM) of tert-butyl 4-(hydroxymethylthiomethyl)piperidine-1-carboxylate and 1.51 ml (10.8 mM) of triethylamine in 30 ml of tetrahydrofuran with ice-cooling, stirring the mixture at the prevailing temperature for 0.5 hour, pouring the mixture in water, extracting it with 2 portions of ethyl acetate, drying the pooled organic layer over MgSO4, and concentrating it], and the mixture was refluxed for 3 hours. The solvent was distilled off under reduced pressure and the residue was diluted with water and extracted with 2 portions of ethyl acetate. The organic layers were pooled and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate: 3/1 to ethyl acetate) to provide the title compound.

後処理

  1. temperaturecooling
  2. customwas prepared
  3. temperaturecooling
  4. stirringstirring the mixture at the prevailing temperature for 0.5 hour
  5. extractionextracting it with 2 portions of ethyl acetate
  6. dry with materialdrying the pooled organic layer over MgSO4
  7. concentrationconcentrating it], and the mixture
  8. temperaturewas refluxed for 3 hours
  9. distillationThe solvent was distilled off under reduced pressure
  10. additionthe residue was diluted with water
  11. extractionextracted with 2 portions of ethyl acetate
  12. dry with materialdried over MgSO4
  13. distillationthe solvent was distilled off under reduced pressure
  14. customThe residue was purified by silica gel column chromatography (hexane-ethyl acetate: 3/1 to ethyl acetate)

出典と根拠

ORDレコード
ord-cec811c9c7bf4f8eb76c5cd3130d7d9f
出典データセット
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06235731B1

反応ノート

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