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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178432322, 화합물 → HCID 178432321, 화합물

HRID 220782
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HRID 220782 반응식
C([N:9]1[CH2:18][CH2:17][C:16]2[N:15]=[C:14]([CH3:19])[NH:13][C:12]=2[C:11]2[CH:20]=[CH:21][CH:22]=[CH:23][C:10]1=2)(=O)C1C=CC=CC=1>Cl.O1CCOCC1>[CH3:19][C:14]1[NH:13][C:12]2[C:11]3[CH:20]=[CH:21][CH:22]=[CH:23][C:10]=3[NH:9][CH2:18][CH2:17][C:16]=2[N:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178432322HCID 178432322, 화합물

생성물 1

HCID 178432321HCID 178432321, 화합물수율 66%

시약·촉매·용매 1

HCID 204431481,4-Dioxane hydrochloride용매

실험 절차

6-Benzoyl-2-methyl-1,4,5,6-tetrahydro-1,3,6-triaza-benzo[e]azulene from Example E5.8 (160 mg, 0.53 mmol) was dissolved in a 6M HCl/dioxan solution (50 ml) and heated at reflux for 18 h. The reaction mixture was cooled to room temperature and reduced in vacuo. The residue was partitioned between EtOAc and saturated NaHCO3 (aq) and the layers were separated. The organic layer was washed with brine, dried, filtered and reduced in vacuo to yield the title compound (69 mg, 66%).

후처리

  1. temperatureheated
  2. temperatureat reflux for 18 h
  3. customThe residue was partitioned between EtOAc and saturated NaHCO3 (aq)
  4. customthe layers were separated
  5. washThe organic layer was washed with brine
  6. customdried
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-c1733d20b31143ce812564b0425f889a
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202858B2

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