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1,4-Dioxane hydrochloride → 3,3-Difluoro-1,6-diaza-spiro[3.5]nonane-1-carboxylic acid benzyl ester

HRID 1912420
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인쇄 미리보기

반응식

HRID 1912420 반응식
C(OC([N:8]1[CH2:28][CH2:27][CH2:26][C:10]2([N:13]([C:14]([O:16][CH2:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[O:15])[CH2:12][C:11]2([F:25])[F:24])[CH2:9]1)=O)(C)(C)C.Cl.O1CCOCC1>>[CH2:17]([O:16][C:14]([N:13]1[C:10]2([CH2:26][CH2:27][CH2:28][NH:8][CH2:9]2)[C:11]([F:25])([F:24])[CH2:12]1)=[O:15])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 204431481,4-Dioxane hydrochlorideHCID 582933383,3-Difluoro-1,6-diaza-spiro[3.5]nonane-1,6-dicarboxylic acid 1-benzyl ester 6-tert-butyl ester

생성물 1

HCID 582933343,3-Difluoro-1,6-diaza-spiro[3.5]nonane-1-carboxylic acid benzyl ester수율 118.9%

실험 절차

To an optically-active compound of 3,3-difluoro-1,6-diaza-spiro[3.5]nonane-1,6-dicarboxylic acid 1-benzyl ester 6-tert-butyl ester (12.6 g) was added 4M hydrochloric acid-1,4-dioxane (126 ml), and the mixture was stirred at room temperature for 30 minutes. The mixture was concentrated under reduced pressure, and thereto was added toluene. The mixture was concentrated under reduced pressure again to give the titled compound (11.2 g).

후처리

concentration
The mixture was concentrated under reduced pressure
  • additionwas added toluene
  • concentrationThe mixture was concentrated under reduced pressure again
  • 출처 및 근거

    ORD 기록
    ord-c6e78e19a0d7407681b64adec43841b6
    출처 데이터셋
    uspto-grants-2013_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08609647B2

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