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Sodium Azide → HCID 86600237, 화합물

HRID 859892
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HRID 859892 반응식
[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]
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참가 물질

4

반응물 2

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

생성물 1

HCID 86600237HCID 86600237, 화합물수율 84.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
120 °C

실험 절차

(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.

후처리

  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)

출처 및 근거

ORD 기록
ord-fe5118d282ee4bb797fb4c82d932b075
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07153851B2

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