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Tetrahydrofuran → Ethyl 4-[1-[(10-(methoxymethyl)-10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl]carbamoyl]piperidin-4-yl]-2-methylbutanoate

HRID 1059364
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HRID 1059364 반응식
[N:1]1[C:10]2[NH:9][C:8]3[CH:11]=[C:12]([CH2:15]C(O)=O)[CH:13]=[CH:14][C:7]=3[S:6][C:5]=2[N:4]=[CH:3][CH:2]=1.C([N:21]([CH2:24]C)CC)C.[N-]=[N+]=[N-].P([O-])(OC1C=CC=CC=1)(OC1C=CC=CC=1)=[O:30].[NH:46]1[CH2:51][CH2:50][CH:49]([CH2:52][CH2:53][CH:54]([CH3:60])[C:55]([O:57][CH2:58][CH3:59])=[O:56])[CH2:48][CH2:47]1.[O:61]1[CH2:65]CC[CH2:62]1>C(OCC)(=O)C>[CH3:62][O:61][CH2:65][N:9]1[C:8]2[CH:11]=[C:12]([CH2:15][NH:21][C:24]([N:46]3[CH2:51][CH2:50][CH:49]([CH2:52][CH2:53][CH:54]([CH3:60])[C:55]([O:57][CH2:58][CH3:59])=[O:56])[CH2:48][CH2:47]3)=[O:30])[CH:13]=[CH:14][C:7]=2[S:6][C:5]2[N:4]=[CH:3][CH:2]=[N:1][C:10]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 11298836Ethyl 4-(piperidin-4-yl)-2-methylbutanoateHCID 1867013310H-Pyrazino[2,3-b][1,4]benzothiazine-8-acetic acidHCID 21964642Diphenylphosphate azide

생성물 1

HCID 18670562
Ethyl 4-[1-[(10-(methoxymethyl)-10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl]carbamoyl]piperidin-4-yl]-2-methylbutanoate

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 0.7 g of 10H-pyrazino[2,3-b][1,4]benzothiazine-8-acetic acid in tetrahydrofuran (50 ml) were added 0.35 ml of triethylamine and 0.55 ml of diphenyl phosphate azide and the resulting mixture was stirred at room temperature for 3 hours. Next, it was heated under reflux for 1.5 hours. After adding 0.55 g of ethyl 4-(piperidin-4-yl)-2-methylbutanoate, the resulting mixture was reacted at room temperature for 1 hour. After adding ethyl acetate, the reaction mixture was washed with water and dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluted with dichloromethane/methanol) to thereby give 0.66 g of the title compound as a yellow oily substance.

후처리

  1. temperatureNext, it was heated
  2. temperatureunder reflux for 1.5 hours
  3. customthe resulting mixture was reacted at room temperature for 1 hour
  4. washthe reaction mixture was washed with water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationAfter distilling off the solvent under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (eluted with dichloromethane/methanol)

출처 및 근거

ORD 기록
ord-e7bbc59923dd46089f7334316f7b69c9
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518423B1

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