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p-Toluenesulfonic acid → 3,3a-Dihydropyrrolo[1,2-a]quinoxaline-1,4(2H,5H)-dione

HRID 1378768
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HRID 1378768 반응식
C[O:2][C:3](=O)[CH:4]([CH2:15][CH2:16][C:17]([O:19]C)=O)[NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N+:12]([O-])=O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CO.[Pd]>[C:17]1(=[O:19])[N:5]2[C:6]3[C:7]([NH:12][C:3](=[O:2])[CH:4]2[CH2:15][CH2:16]1)=[CH:8][CH:9]=[CH:10][CH:11]=3
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 10357193HCID 10357193, 화합물

생성물 1

HCID 2581143,3a-Dihydropyrrolo[1,2-a]quinoxaline-1,4(2H,5H)-dione

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To N-(2-nitrophenyl)-DL-glutamic acid dimethyl ester (XI, EXAMPLE 279, 5.09 g) in methanol (150 ml) is added p-toluenesulfonic acid (0.158 g) and palladium on carbon (10%, 0.495 g). The mixture is shaken under hydrogen at 37 psi for 2 hr; the mixture is then filtered and the filtrate is concentrated to about 70 ml. Additional p-toluenesulfonic acid (0.15 g) is added, and the solution is heated at 60° for 1 hr. After cooling, the solid is collected, washed with methanol, and dried to give the title compound, mp 231°-232°; NMR (CDCl3) 2.65, 4.41, 6.93, 7.14, 8.10 and 8.55 δ.

후처리

  1. filtrationthe mixture is then filtered
  2. concentrationthe filtrate is concentrated to about 70 ml
  3. additionAdditional p-toluenesulfonic acid (0.15 g) is added
  4. temperaturethe solution is heated at 60° for 1 hr
  5. temperatureAfter cooling
  6. customthe solid is collected
  7. washwashed with methanol
  8. customdried

출처 및 근거

ORD 기록
ord-7b897e347c61408e877a61fadbdf74a3
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05668282

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