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Methanol → 4-(Furan-2-yl)-1,3-thiazol-2-amine

HRID 737184
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HRID 737184 반응식
Br[C:2]1[N:3]=[C:4]([NH2:7])[S:5][CH:6]=1.[O:8]1[CH:12]=[CH:11][CH:10]=[C:9]1B(O)O.CO.C([O-])(O)=O.[Na+]>CN(C=O)C>[O:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[C:2]1[N:3]=[C:4]([NH2:7])[S:5][CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 4280244-Bromo-1,3-thiazol-2-amineHCID 516892Sodium BicarbonateHCID 2734357Furan-2-boronic acid

생성물 1

HCID 7278344-(Furan-2-yl)-1,3-thiazol-2-amine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
70 °C

실험 절차

4-Bromo-thiazol-2-ylamine (100 mg, 0.34 mmol) was combined with 57 mg (0.51 mmol) of 2-furan boronic acid. To this mixture was added 5 mL of MeOH, 1 mL of sat. NaHCO3 (aq), and 0.8 mL of DMF. Reaction mixture was degassed and Pd[P(Ph)3]4 (25 mg) was added. Reaction mixture was heated at 70° C. for 7 hours. The reaction mixture was brought to room temperature and filtered. The filtrate was evaporated and purified using reverse phase HPLC.

후처리

  1. customReaction mixture
  2. customwas degassed
  3. additionPd[P(Ph)3]4 (25 mg) was added
  4. customReaction mixture
  5. customwas brought to room temperature
  6. filtrationfiltered
  7. customThe filtrate was evaporated
  8. custompurified

출처 및 근거

ORD 기록
ord-d72521ecc2654be1960ae04b50ff8c01
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07595398B2

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