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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1H-1,2,4-Triazole → 6-((2R,6R)-2,6-dimethylmorpholino)-7-fluoro-3-(1H-1,2,4-triazol-1-yl)benzo[d]isoxazole-5-carbaldehyde

HRID 245543
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HRID 245543 반응식
[H-].[Na+].[NH:3]1[CH:7]=[N:6][CH:5]=[N:4]1.Cl[C:9]1[C:13]2[CH:14]=[C:15]([CH:27]=[O:28])[C:16]([N:19]3[CH2:24][C@@H:23]([CH3:25])[O:22][C@H:21]([CH3:26])[CH2:20]3)=[C:17]([F:18])[C:12]=2[O:11][N:10]=1>CN(C=O)C.C(Cl)Cl>[CH3:26][C@@H:21]1[CH2:20][N:19]([C:16]2[C:15]([CH:27]=[O:28])=[CH:14][C:13]3[C:9]([N:3]4[CH:7]=[N:6][CH:5]=[N:4]4)=[N:10][O:11][C:12]=3[C:17]=2[F:18])[CH2:24][C@@H:23]([CH3:25])[O:22]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 92571H-1,2,4-TriazoleHCID 24758Sodium hydrideHCID 866581223-chloro-6-((2R,6R)-2,6-dimethylmorpholino)-7-fluorobenzo[d]isoxazole-5-carbaldehyde2회

생성물 1

HCID 866581356-((2R,6R)-2,6-dimethylmorpholino)-7-fluoro-3-(1H-1,2,4-triazol-1-yl)benzo[d]isoxazole-5-carbaldehyde

시약·촉매·용매 2

HCID 6228Dimethylformamide용매
HCID 6344Dichloromethane용매

실험 절차

Sodium hydride (60% dispersion) (0.288 g, 7.19 mmol) was added to a solution of 1H-1,2,4-triazole (0.530 g, 7.67 mmol) and 3-chloro-6-((2R,6R)-2,6-dimethylmorpholino)-7-fluorobenzo[d]isoxazole-5-carbaldehyde (Intermediate 535, 1.5 g, 4.80 mmol) in DMF (10 ml), and the mixture was stirred at room temperature overnight. The mixture was quenched with aqueous NH4Cl and diluted with water before being extracted with CH2Cl2 5 times. The combined extracts were dried (MgSO4) and concentrated to give a solid that was taken up in CH2Cl2. Insoluble solids were filtered off and rinsed with additional CH2Cl2. The solids were dried in vacuo and were consistent with desired product. The filtrate was concentrated and chromatographed on silica gel (100% CH2Cl2 followed by gradient elution to 50% EtOAc in CH2Cl2) to give additional desired product. Total of 866 mg.

후처리

  1. customThe mixture was quenched with aqueous NH4Cl
  2. additiondiluted with water
  3. extractionbefore being extracted with CH2Cl2 5 times
  4. dry with materialThe combined extracts were dried (MgSO4)
  5. concentrationconcentrated
  6. customto give a solid
  7. filtrationInsoluble solids were filtered off
  8. washrinsed with additional CH2Cl2
  9. customThe solids were dried in vacuo
  10. concentrationThe filtrate was concentrated
  11. customchromatographed on silica gel (100% CH2Cl2 followed by gradient elution to 50% EtOAc in CH2Cl2)

출처 및 근거

ORD 기록
ord-57f57cbfbe1e4320ad9cb5c00301d120
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658641B2

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