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Sodium Azide → HCID 86600237、化合物

HRID 859892
ノート
印刷プレビュー

反応式

HRID 859892 の反応式
[CH2:1]([N:8]1[CH2:12][C@H:11]([CH2:13]OS(C)(=O)=O)[C@@H:10]([OH:19])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N-:20]=[N+:21]=[N-:22].[Na+]>CN(C)C=O>[N:20]([CH2:13][C@@H:11]1[C@@H:10]([OH:19])[CH2:9][N:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:12]1)=[N+:21]=[N-:22]
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

4

反応物 2

HCID 33557Sodium AzideHCID 86600238(3R,4R)-1-Benzyl-3-hydroxy-4-methanesulfonyloxymethylpyrrolidine

生成物 1

HCID 86600237HCID 86600237、化合物収率 84.7%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
120 °C

実験手順

(3R,4R)-1-Benzyl-3-hydroxy-4-methanesulfonyloxymethylpyrrolidine (835 mg), sodium azide (381 mg), and N,N-dimethylformamide (12 mL) were mixed with one another and the mixture was stirred at 120° C. for 1 hour. Subsequently, the reaction mixture was concentrated under reduced pressure. To the resulting residue, water (10 mL) was added and the mixture was extracted with diethyl ether (2×30 mL). The diethyl ether extracts were combined and the combined extract was dried over anhydrous sodium sulfate and was concentrated under reduced pressure. The resulting residue was purified on a silica gel column (eluant=ethyl acetate: methanol=20:1) to give 576 mg of (3R,4R)-3-azidomethyl-1-benzyl-4-hydroxypyrrolidine as a pale brown oil.

後処理

  1. concentrationSubsequently, the reaction mixture was concentrated under reduced pressure
  2. additionTo the resulting residue, water (10 mL) was added
  3. extractionthe mixture was extracted with diethyl ether (2×30 mL)
  4. extractionthe combined extract
  5. dry with materialwas dried over anhydrous sodium sulfate
  6. concentrationwas concentrated under reduced pressure
  7. customThe resulting residue was purified on a silica gel column (eluant=ethyl acetate: methanol=20:1)

出典と根拠

ORDレコード
ord-fe5118d282ee4bb797fb4c82d932b075
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07153851B2

反応ノート

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