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Hydrochloric Acid → (5R)-3-{4-[5-(Dimethoxymethyl)-1-methyl-1H-pyrazol-3-yl]phenyl}-5-(hydroxymethyl)-1,3-oxazolidin-2-one

HRID 456794
ノート
印刷プレビュー

反応式

HRID 456794 の反応式
[CH2:1]([O:3][CH:4]([O:28][CH2:29]C)[C:5]1[N:9]([CH3:10])[N:8]=[C:7]([C:11]2[CH:16]=[CH:15][C:14]([NH:17][C:18](=[O:27])[O:19][CH2:20][C:21]3C=CC=CC=3)=[CH:13][CH:12]=2)[CH:6]=1)C.[Li]CCCC.[C:36](OC[C@H]1CO1)(=[O:40])CCC.Cl.C(OC)(OC)OC>C1COCC1.C12(CS(O)(=O)=O)C(C)(C)C(CC1)CC2=O.C(N(CC)CC)C.CO>[CH3:1][O:3][CH:4]([O:28][CH3:29])[C:5]1[N:9]([CH3:10])[N:8]=[C:7]([C:11]2[CH:16]=[CH:15][C:14]([N:17]3[CH2:21][C@H:20]([CH2:36][OH:40])[O:19][C:18]3=[O:27])=[CH:13][CH:12]=2)[CH:6]=1
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 313Hydrochloric AcidHCID 9005Trimethyl orthoformateHCID 2724536(2R)-Oxiran-2-ylmethyl butanoateHCID 18438601Benzyl 4-[5-(diethoxymethyl)-1-methyl-1H-pyrazol-3-yl]phenylcarbamate2 回HCID 178418339Butyllithium

生成物 1

HCID 58625204
(5R)-3-{4-[5-(Dimethoxymethyl)-1-methyl-1H-pyrazol-3-yl]phenyl}-5-(hydroxymethyl)-1,3-oxazolidin-2-one
収率 49.5%

試薬・触媒・溶媒 4

HCID 18462Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-触媒HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒2 回HCID 8471Triethylamine溶媒

実験手順

Benzyl 4-[5-(diethoxymethyl)-1-methyl-1H-pyrazol-3-yl]phenylcarbamate (Intermediate 11, 8.29 g, 20.2 mmol), was dissolved in THF (150 ml) and cooled to −70° C. nBuLi (15 ml of a 1.6 M solution in hexanes, 24 mmol) was added dropwise over 10 min. After 25 min at −70° C., (2R)-oxiran-2-ylmethyl butyrate (3.7 ml, 26.2 mmol) was added and the solution was allowed to warm slowly to room temperature over 16 hours. The mixture was poured into 0.25M HCl and extracted with ethyl acetate, the organic layer was washed with saturated NaCl, dried over sodium sulfate and evaporated to give the crude product which was partially hydrolysed to the aldehyde. The crude product was dissolved in 1:1 THF:methanol (12 ml), trimethyl orthoformate (2.6 ml, 24 mmol) and camphorsulfonic acid (100 mg, 0.4 mmol) were added and the solution was warmed at 50° C. for 1 hour. Triethylamine (0.5 ml) was added and the solution was evaporated and purified by chromatography on silica gel, eluting with 60–100% ethyl acetate/hexane, to give the title compound as a white solid (3.47 g).

後処理

  1. additionwas added dropwise over 10 min
  2. extractionextracted with ethyl acetate
  3. washthe organic layer was washed with saturated NaCl
  4. dry with materialdried over sodium sulfate
  5. customevaporated
  6. customto give the crude product which
  7. temperaturethe solution was warmed at 50° C. for 1 hour
  8. customthe solution was evaporated
  9. custompurified by chromatography on silica gel
  10. washeluting with 60–100% ethyl acetate/hexane

出典と根拠

ORDレコード
ord-a2da76024d3a46f38ea9689dda5da567
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07186738B2

反応ノート

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