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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → N-{2,4-Dimethyl-5-[6-(pyridin-3-yl)-1H-imidazo[1,2-b]pyrazol-1-yl]phenyl}-3-(methoxymethyl)-5-(pentafluoro-lambda6-sulphanyl)benzamide

HRID 1055755
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HRID 1055755 반응식
[CH3:1]N(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C[C:26]1[C:32]([N:33]2[C:40]3[N:36]([N:37]=[C:38]([C:41]4[CH:42]=[N:43][CH:44]=[CH:45][CH:46]=4)[CH:39]=3)[CH:35]=[CH:34]2)=[C:31]([CH3:47])[CH:30]=[CH:29][C:27]=1[NH2:28].[CH3:48][O:49][CH2:50][C:51]1[CH:52]=[C:53]([CH:57]=[C:58]([S:60]([F:65])([F:64])([F:63])([F:62])[F:61])[CH:59]=1)[C:54](O)=[O:55]>CN(C=O)C.CO>[CH3:1][C:29]1[CH:30]=[C:31]([CH3:47])[C:32]([N:33]2[C:40]3[N:36]([N:37]=[C:38]([C:41]4[CH:42]=[N:43][CH:44]=[CH:45][CH:46]=4)[CH:39]=3)[CH:35]=[CH:34]2)=[CH:26][C:27]=1[NH:28][C:54](=[O:55])[C:53]1[CH:57]=[C:58]([S:60]([F:65])([F:64])([F:63])([F:62])[F:61])[CH:59]=[C:51]([CH2:50][O:49][CH3:48])[CH:52]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 89699939HCID 89699939, 화합물HCID 897000823-(Methoxymethyl)-5-(pentafluoro-lambda6-sulphanyl)benzoic acid

생성물 1

HCID 89699909N-{2,4-Dimethyl-5-[6-(pyridin-3-yl)-1H-imidazo[1,2-b]pyrazol-1-yl]phenyl}-3-(methoxymethyl)-5-(pentafluoro-lambda6-sulphanyl)benzamide

시약·촉매·용매 2

HCID 887Methanol용매HCID 6228Dimethylformamide용매

실험 절차

75 mg (0.198 mmol) of HATU, 24 mg (0.198 mmol) of 4-N,N-dimethylaminopyridine (DMAP) and 50 mg (0.165 mmol) of the compound of Example 11A were added to a solution of 51 mg (0.173 mmol) of the compound of Example 74A in 1 ml of anhydrous DMF. The reaction mixture was stirred at RT for 1 h, then diluted with about 2 ml of methanol and subsequently directly separated into its components by preparative HPLC (Method 32). Evaporation of the product fractions and drying of the residue under high vacuum gave 60 mg (63% of theory) of the title compound.

후처리

  1. customsubsequently directly separated into its components by preparative HPLC (Method 32)
  2. customEvaporation of the product fractions
  3. customdrying of the residue under high vacuum

출처 및 근거

ORD 기록
ord-eac742d9687f4defa024ff7f7a338c4f
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394309B2

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