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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → HCID 11831504, 화합물

HRID 1067593
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HRID 1067593 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[C:9]([C:11]([CH3:16])([CH3:15])[C:12](O)=[O:13])[N:10]=2)[N:7]=1.[Cl-].[NH4+].C([N:21](CC)CC)C>CN(C)C=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[C:9]([C:11]([CH3:16])([CH3:15])[C:12]([NH2:21])=[O:13])[N:10]=2)[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 25517Ammonium ChlorideHCID 11746720HCID 11746720, 화합물

생성물 1

HCID 11831504HCID 11831504, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

1.20 g of 2-(6-chloroimidazo[1,2-b]pyridazin-2-yl)-2-methylpropionic acid was dissolved in 8 ml of N,N-dimethylformamide; 0.892 g of N,N′-carbonyldiimidazole was added, followed by stirring at room temperature for 30 minutes. To this mixture, 0.321 g of ammonium chloride and 0.832 ml of triethylamine were added under ice cooling conditions, followed by stirring at room temperature for 3 hours. Ice water was added to the reaction mixture; the crystal precipitated was collected by filtration, washed with water and dried to yield 0.697 g of the title compound.

후처리

  1. stirringby stirring at room temperature for 3 hours
  2. customthe crystal precipitated
  3. filtrationwas collected by filtration
  4. washwashed with water
  5. customdried

출처 및 근거

ORD 기록
ord-8a90a1f206bd4de289da78ea7818424f
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06248740B1

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