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(+/-)-N-{3-[2,4-bis(methoxymethoxy)phenyl]cyclohexyl}acetamide → (+/-)-N-[3-(2,4-dihydroxyphenyl)cyclohexyl]acetamide

HRID 585715
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반응식

HRID 585715 반응식
COC[O:4][C:5]1[CH:10]=[C:9]([O:11]COC)[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:20][CH2:19][CH2:18][CH:17]([NH:21][C:22](=[O:24])[CH3:23])[CH2:16]1>CO>[OH:4][C:5]1[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:20][CH2:19][CH2:18][CH:17]([NH:21][C:22](=[O:24])[CH3:23])[CH2:16]1
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참가 물질

3

반응물 1

HCID 22337801(+/-)-N-{3-[2,4-bis(methoxymethoxy)phenyl]cyclohexyl}acetamide

생성물 1

HCID 22337784(+/-)-N-[3-(2,4-dihydroxyphenyl)cyclohexyl]acetamide수율 34%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

(±)-N-{3-[2,4-bis(methoxymethoxy)phenyl]cyclohexyl}acetamide (20 mg), methanol (2 ml) and acidic ion exchange resin (300 mg) were heated under reflux for 3 hr. The reaction mixture was filtered and the resin was washed with methanol. The combined filtrate and washings were evaporated in vacuo and the crude residue was purified by preparative HPLC to furnish the title compound as a solid (5 mg, 34%). δH (CD3OD) 1.10-2.00 (11H, m), 2.90 (0.3H, tt), 3.08 (0.7H, tt), 3.70-3.80 (0.3H, m), 4.16 (0.7H, m), 6.20-6.26 (2H, m), 6.84-6.90 (1H, m); m/z (ES+) 250 (M+H)+.

후처리

  1. temperatureunder reflux for 3 hr
  2. filtrationThe reaction mixture was filtered
  3. washthe resin was washed with methanol
  4. customThe combined filtrate and washings were evaporated in vacuo
  5. customthe crude residue was purified by preparative HPLC

출처 및 근거

ORD 기록
ord-62ae0161374a44dcba0f3610e84cf3ce
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06933319B2

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