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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → (+/-) N-(3-{[2-(10-Aza-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-methanesulfonamide

HRID 1161647
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HRID 1161647 반응식
C[N:2]([C:7]1[C:12]([CH2:13][NH:14][C:15]2[C:20]([C:21]([F:24])([F:23])[F:22])=[CH:19][N:18]=[C:17]([NH:25][C:26]3[CH:36]=[CH:35][C:34]4[CH:33]5[CH2:37][CH:29]([CH2:30][N:31](C(=O)C(F)(F)F)[CH2:32]5)[C:28]=4[CH:27]=3)[N:16]=2)=[CH:11][CH:10]=[CH:9][N:8]=1)[S:3]([CH3:6])(=[O:5])=[O:4].[OH-].[Na+]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.O1CCCC1>[CH:29]12[CH2:37][CH:33]([CH2:32][NH:31][CH2:30]1)[C:34]1[CH:35]=[CH:36][C:26]([NH:25][C:17]3[N:16]=[C:15]([NH:14][CH2:13][C:12]4[C:7]([NH:2][S:3]([CH3:6])(=[O:4])=[O:5])=[N:8][CH:9]=[CH:10][CH:11]=4)[C:20]([C:21]([F:22])([F:23])[F:24])=[CH:19][N:18]=3)=[CH:27][C:28]2=1
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 86623360(+/-) N-Methyl-N-(3-{[2-(10-trifluoroacetyl-10-aza-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-methanesulfonamide

생성물 1

HCID 68693452(+/-) N-(3-{[2-(10-Aza-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-methanesulfonamide

시약·촉매·용매 2

HCID 66133
Benzyl triethylammonium chloride
촉매
HCID 8028Tetrahydrofuran용매

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온도
70 °C

실험 절차

A solution 3 and tetrahydrofuran (2.00 mL) was treated with three crystals of benzyl triethyl ammonium chloride and 40% aqueous NaOH (2.00 mL), and the resultant bi-phasic reaction was heated to 70° C. under nitrogen. After sixteen hours, the mixture was allowed to cool to 25° C. The organic phase was collected and the aqueous layer was washed with EtOAc. The combined organic phases were dried over MgSO4, concentrated under reduced pressure, and purified over silica (92:8:0.8 CHCl3:CH3OH: NH4OH) to provide 32 g of 4 as a yellow foam). The yellow foam was dissolved in a minimum amount of CH2Cl2 at ° C., and 15 μL (0.0600 mmol) of 4.0 M HCl in 1,4-dioxane was slowly added. The resultant white slurry was stirred under a gentle flow of nitrogen for one hour and filtered to provide the hydrochloride salt from of 4 as a white solid (25 mg, 0.0474 mmol, 38%). C24H26F3N7O2S HPLC r.t.=5.10 min.; LC/MS (Method F) m/z 534.4 (MH+).

후처리

  1. customthe resultant bi-phasic reaction
  2. waitAfter sixteen hours
  3. temperatureto cool to 25° C
  4. customThe organic phase was collected
  5. washthe aqueous layer was washed with EtOAc
  6. dry with materialThe combined organic phases were dried over MgSO4
  7. concentrationconcentrated under reduced pressure
  8. custompurified over silica (92:8:0.8 CHCl3:CH3OH: NH4OH)

출처 및 근거

ORD 기록
ord-7ea7e166242545539ce93d4059e44f3a
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820648B2

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