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Methanol → N-(1-{4-[(hydroxyamino)carbonyl]phenyl}-2-methylpropyl)adamantane-1-carboxamide

HRID 1049090
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HRID 1049090 반응식
[C:1]12([C:11]([NH:13][CH:14]([C:18]3[CH:28]=[CH:27][C:21]([C:22]([O:24]CC)=O)=[CH:20][CH:19]=3)[CH:15]([CH3:17])[CH3:16])=[O:12])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[OH-:29].[K+].Cl.[NH2:32]O.CO>C(O)(=O)C>[OH:29][NH:32][C:22]([C:21]1[CH:20]=[CH:19][C:18]([CH:14]([NH:13][C:11]([C:1]23[CH2:10][CH:5]4[CH2:4][CH:3]([CH2:9][CH:7]([CH2:6]4)[CH2:8]2)[CH2:2]3)=[O:12])[CH:15]([CH3:16])[CH3:17])=[CH:28][CH:27]=1)=[O:24]
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참가 물질

6

반응물 4

HCID 887MethanolHCID 14797Potassium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 67396119Ethyl 4-{1-[(adamantan-1-ylcarbonyl)amino]-2-methylpropyl}benzoate

생성물 1

HCID 58417123N-(1-{4-[(hydroxyamino)carbonyl]phenyl}-2-methylpropyl)adamantane-1-carboxamide수율 15%

시약·촉매·용매 1

HCID 176
Acetic Acid
용매

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온도
80 °C

실험 절차

To the crude ethyl 4-{1-[(adamantan-1-ylcarbonyl)amino]-2-methylpropyl}benzoate in a vial was added potassium hydroxide (0.11 g, 1.87 mmol), hydroxylamine hydrochloride (0.047 g, 0.68 mmol), and methanol (2 mL). The reaction was capped and heated at 80° C. for 1 h. After cooled to rt, acetic acid (0.097 mL, 1.7 mmol was added to neutralize the excess base. The solvent was then completely evaporated. To the solid was added DMSO (1.3 mL). The solution was then filtered and purified by prep-HPLC purification to give the title compound (0.009 g, 15%) as a white solid. LC-MS: (FA) ES+ 371.

후처리

  1. customThe reaction was capped
  2. temperatureAfter cooled to rt
  3. customThe solvent was then completely evaporated
  4. additionTo the solid was added DMSO (1.3 mL)
  5. filtrationThe solution was then filtered
  6. custompurified by prep-HPLC purification

출처 및 근거

ORD 기록
ord-49d042249e7a4cf19e355bae2fadd751
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09382197B2

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