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Morpholine → HCID 67756016, 화합물

HRID 2372386
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HRID 2372386 반응식
[CH:1]([O:4][C:5]([C:7]1[C:8]([CH3:19])=[CH:9][N:10]2[CH:14]([CH2:15][C:16]([OH:18])=O)[CH2:13][S:12][C:11]=12)=[O:6])([CH3:3])[CH3:2].[NH:20]1[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1.C1(N=C=NC2CCCCC2)CCCCC1>ClCCl>[CH:1]([O:4][C:5]([C:7]1[C:8]([CH3:19])=[CH:9][N:10]2[CH:14]([CH2:15][C:16]([N:20]3[CH2:25][CH2:24][O:23][CH2:22][CH2:21]3)=[O:18])[CH2:13][S:12][C:11]=12)=[O:6])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8083MorpholineHCID 10868DicyclohexylcarbodiimideHCID 19903387HCID 19903387, 화합물

생성물 1

HCID 67756016HCID 67756016, 화합물수율 54.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1.54 g of (7-isopropoxycarbonyl-6-methyl-2,3-dihydropyrrolo[2,1-b]thiazol-3-yl)acetic acid, 0.70 g of morpholine and 0.12 g of 4-N,N-dimethylaminopyridine were dissolved in 50 ml of dichloromethane. 1.44 g of N,N'-dicyclohexylcarbodiimide was added thereto under ice-cooling and stirring. Then the mixture was stirred at room temperature for 9 days. After filtering off the insoluble matters, the solvent was distilled off. The oily residue thus obtained was purified by silica gel column chromatography. After crystallizing from ether/n-hexane, 1.05 g of the title compound was obtained.

후처리

  1. temperatureunder ice-cooling
  2. stirringThen the mixture was stirred at room temperature for 9 days
  3. filtrationAfter filtering off the insoluble matters
  4. distillationthe solvent was distilled off
  5. customThe oily residue thus obtained
  6. customwas purified by silica gel column chromatography
  7. customAfter crystallizing from ether/n-hexane

출처 및 근거

ORD 기록
ord-7d04c969db48418d81b8d8d3fc24d692
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05098919

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