홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Tetrafluoroboric acid → HCID 178481919, 화합물

HRID 72703
노트
인쇄 미리보기

반응식

HRID 72703 반응식
[CH3:1][N:2]1[C:6]2=[N:7][CH:8]=[N:9][C:10]([OH:11])=[C:5]2[CH:4]=[N:3]1.[I:12]N1C(=O)CCC1=O.F[B-](F)(F)F.[H+].C(=O)(O)[O-].[Na+]>C(#N)C.O>[I:12][C:4]1[C:5]2[C:6](=[N:7][CH:8]=[N:9][C:10]=2[OH:11])[N:2]([CH3:1])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 28118Tetrafluoroboric acidHCID 120273N-IodosuccinimideHCID 516892Sodium BicarbonateHCID 178481767HCID 178481767, 화합물

생성물 1

HCID 178481919HCID 178481919, 화합물

시약·촉매·용매 2

HCID 962Water용매
HCID 6342
Acetonitrile
용매

실험 절차

1-Methyl-1H-pyrazolo[3,4-d]pyrimidin-4-ol (5.50 g, 36.6 mmol) was combined with N-iodosuccinimide (97%, 12.7 g, 54.8 mmol) and tetrafluoroboric acid (50% solution in water, 23.0 mL, 183 mmol) in acetonitrile (50 mL) and the reaction mixture was heated to reflux for 5 hours. After cooling to room temperature, the reaction mixture was poured portion-wise into water (50 mL) containing sodium bicarbonate (18.6 g, 220 mmol). When gas evolution had ceased, the mixture was filtered, and the dark solid was washed successively with saturated aqueous sodium thiosulfate solution (25 mL) and water (2×25 mL). The resulting solid was dried under vacuum overnight at 50° C. to afford the product as a cream-colored solid. Yield: 9.35 g, 33.9 mmol, 93%. LCMS m/z 277.0 (M+1). 1H NMR (500 MHz, DMSO-d6) δ 3.87 (s, 3H), 8.07 (s, 1H), 12.08 (v br s, 1H).

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 5 hours
  3. filtrationthe mixture was filtered
  4. washthe dark solid was washed successively with saturated aqueous sodium thiosulfate solution (25 mL) and water (2×25 mL)
  5. customThe resulting solid was dried under vacuum overnight at 50° C.

출처 및 근거

ORD 기록
ord-66b0366bb8ec4ba5989d196a35c4a5eb
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829010B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트