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Dimethyl Sulfoxide → [4-((R)-2-formyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid methyl ester

HRID 2052938
ノート
印刷プレビュー

反応式

HRID 2052938 の反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH3:11][O:12][C:13](=[O:29])[CH2:14][O:15][CH2:16][CH2:17][CH2:18][CH2:19][N:20]1[C:25](=[O:26])[CH2:24][CH2:23][CH2:22][C@@H:21]1[CH2:27][OH:28].C(N(CC)CC)C.C([O-])(O)=O.[Na+]>C(Cl)Cl>[CH3:11][O:12][C:13](=[O:29])[CH2:14][O:15][CH2:16][CH2:17][CH2:18][CH2:19][N:20]1[C:25](=[O:26])[CH2:24][CH2:23][CH2:22][C@@H:21]1[CH:27]=[O:28]
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

7

反応物 5

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 516892Sodium BicarbonateHCID 69020934[4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid methyl ester

生成物 1

HCID 86595297[4-((R)-2-formyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid methyl ester
収率 40.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒3 回

反応条件

温度
0 °C

実験手順

A solution of oxalyl chloride (0.15 mL, 1.76 mmol) in CH2Cl2 (11.0 mL) was added to a solution of DMSO (0.16 mL, 2.25 mmol) in CH2Cl2 (1.0 mL) at −78° C. After 15 min at −78° C., a solution of [4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid methyl ester (240 mg, 0.88 mmol) in CH2Cl2 (1.5 mL) was added via cannula. After 20 min at −78° C., triethylamine (0.37 mL, 2.65 mmol) was added. After 20 min at −78° C., the mixture was allowed to warm to 0° C. After 30 min at 0° C., the reaction was allowed to warm to rt. After 45 min at rt, saturated aqueous NaHCO3 (15 mL) was added and the mixture was extracted with CH2Cl2 (3×15 mL). The combined organic phase was dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (40%→70% EtOAc/CH2Cl2, gradient) afforded 96 mg (40%) of [4-((R)-2-formyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid methyl ester.

後処理

  1. waitAfter 20 min at −78° C.
  2. waitAfter 20 min at −78° C.
  3. waitAfter 30 min at 0° C.
  4. temperatureto warm to rt
  5. waitAfter 45 min at rt
  6. extractionthe mixture was extracted with CH2Cl2 (3×15 mL)
  7. dry with materialThe combined organic phase was dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customPurification of the residue by flash column chromatography on silica gel (40%→70% EtOAc/CH2Cl2, gradient)

出典と根拠

ORDレコード
ord-26075595b271446896bb53aa21c7eb4c
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07326716B2

反応ノート

読み込み中…

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