Phenyl Isothiocyanate → HCID 178490875, 화합물

HRID 1478411

반응식

HRID 1478411 반응식
[C:1]1([N:7]=[C:8]=S)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH:10]([C:12]1[N:17]([CH2:18][C:19]2[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=2)[C:16](=[O:27])[N:15]([CH3:28])[C:14](=[O:29])[CH:13]=1)[NH2:11]>CN(C=O)C>[CH3:26][O:25][C:22]1[CH:21]=[CH:20][C:19]([CH2:18][N:17]2[C:12]3[NH:10][N:11]=[C:8]([NH:7][C:1]4[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=4)[C:13]=3[C:14](=[O:29])[N:15]([CH3:28])[C:16]2=[O:27])=[CH:24][CH:23]=1

참가 물질

4

반응 조건

온도
120 °C

실험 절차

Phenyl isothiocyanate (3.9 mL, 32.7 mmol) is added to a suspension of 6-hydrazinyl-1-(4-methoxybenzyl)-3-methylpyrimidine-2,4(1H,3H)-dione (0.45 g, 1.6 mmol) in DMF (12 mL). The reaction mixture is heated at 120° C. for 40 hours, and then evaporated to remove solvent under reduced pressure. The residue is washed with hexanes, and then treated with MeOH (125 mL), and stored at −15° C. for 2 days to give a crystalline solid. The solid is recrystallized from CH3OH-EtOAc to afford 2.5 g of product (Yield: 61%). 1H NMR (400 MHz, DMSO-d6) δ 3.21 (s, 3H), 3.73 (s, 3H), 5.01 (s, 2H), 6.88-7.36 (m, 9H). MS (FAB) m/z 378.3 [M+H]+.

후처리

  1. customevaporated
  2. customto remove solvent under reduced pressure
  3. washThe residue is washed with hexanes
  4. additiontreated with MeOH (125 mL)
  5. customto give a crystalline solid
  6. customThe solid is recrystallized from CH3OH-EtOAc

출처 및 근거

ORD 기록
ord-1c9e6b54c21643ae991f64051141728d
출처 데이터셋
uspto-grants-2016_08
특허 번호
US09403836B2

연결된 노트

불러오는 중…