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Lithium hydroxide, monohydrate → HCID 56658836, 화합물

HRID 1188292
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HRID 1188292 반응식
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[C:14]([C:15]3[CH:20]=[CH:19][C:18]([N:21]4[CH2:25][CH2:24][O:23][C:22]4=[O:26])=[CH:17][CH:16]=3)=[CH:13][CH:12]=[C:11]2[CH2:27][CH2:28][C:29]([O:31]CC)=[O:30])=[C:6]([CH3:34])[CH:5]=1)(=[O:3])[NH2:2].O.[OH-].[Li+]>C1COCC1.O>[C:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[C:14]([C:15]3[CH:16]=[CH:17][C:18]([N:21]4[CH2:25][CH2:24][O:23][C:22]4=[O:26])=[CH:19][CH:20]=3)=[CH:13][CH:12]=[C:11]2[CH2:27][CH2:28][C:29]([OH:31])=[O:30])=[C:6]([CH3:34])[CH:5]=1)(=[O:3])[NH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 67176382HCID 67176382, 화합물

생성물 1

HCID 56658836HCID 56658836, 화합물수율 39%

시약·촉매·용매 1

HCID 21881883Oxolane--water (1/1)용매

실험 절차

To a solution of ethyl 3-(1-(4-carbamoyl-2-methylphenyl)-5-(4-(2-oxooxazolidin-3-yl)phenyl)-1H-pyrrol-2-yl)propanoate (67 mg, 0.15 mmol) in THF/H2O (1 mL, v/v=1/1) was added lithium hydroxide monohydrate (7 mg, 0.15 mmol). The mixture was stirred at room temperature for 6 h. THF was evaporated in vacuo. The residue was acidified to pH=5 with 5% hydrochloric acid, concentrated and purified by prep-TLC to afford the titled compound as a brown solid (24 mg, yield 39%).

후처리

  1. customTHF was evaporated in vacuo
  2. concentrationconcentrated
  3. custompurified by prep-TLC

출처 및 근거

ORD 기록
ord-f2fad542005a4845b59642b290caab8e
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08673961B2

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