Biphenyl-2-ylcarbamic Acid 1-(2-{[4-(4-(1,3-Dioxolan-2-yl)-phenylcarbamoyl)butyl]methylcarbamoyl}ethyl)piperidin-4-yl Ester → Biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-formylphenylcarbamoyl)butyl]methylcarbamoyl}ethyl)piperidin-4-yl ester

HRID 1468514노트

반응식

HRID 1468514 반응식
[O:1]1CCO[CH:2]1[C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13]([CH2:15][CH2:16][CH2:17][CH2:18][N:19]([CH3:46])[C:20]([CH2:22][CH2:23][N:24]2[CH2:29][CH2:28][CH:27]([O:30][C:31](=[O:45])[NH:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)[CH2:26][CH2:25]2)=[O:21])=[O:14])=[CH:8][CH:7]=1>Cl.C(#N)C>[CH:2]([C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13]([CH2:15][CH2:16][CH2:17][CH2:18][N:19]([CH3:46])[C:20]([CH2:22][CH2:23][N:24]2[CH2:25][CH2:26][CH:27]([O:30][C:31](=[O:45])[NH:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)[CH2:28][CH2:29]2)=[O:21])=[O:14])=[CH:8][CH:7]=1)=[O:1]

참가 물질

4

반응 조건

온도
50 °C

실험 절차

A stirred mixture of biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-(1,3-dioxolan-2-yl)phenylcarbamoyl)butyl]methylcarbamoyl}ethyl)piperidin-4-yl ester (3.04 g, 4.84 mmol) in aqueous hydrochloric acid (1 M, 10 mL) and acetonitrile (10 mL) was heated at 50° C. for 2 h. The reaction mixture was concentrated under reduced pressure and saturated aqueous sodium bicarbonate solution and DCM were added to the residue. The layers were separated and the organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound (2.83 g, 100% yield).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure and saturated aqueous sodium bicarbonate solution and DCM
  2. additionwere added to the residue
  3. customThe layers were separated
  4. dry with materialthe organic layer was dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-fa88263896684ee29102f7f02a0e9cf4
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09000173B2

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