Dimethylformamide → N-(1,3-Dimethyl-5-pyrazolyl)anthranilic acid

HRID 977136

반응식

HRID 977136 반응식
I[C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[NH2:11][C:12]1[N:16]([CH3:17])[N:15]=[C:14]([CH3:18])[CH:13]=1.CN(C=O)C.C([O-])([O-])=O.[K+].[K+]>CC([O-])=O.CC([O-])=O.[Cu+2].C(O)(=O)C>[CH3:17][N:16]1[C:12]([NH:11][C:2]2[C:3](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4]([OH:6])=[O:5])=[CH:13][C:14]([CH3:18])=[N:15]1

참가 물질

7

반응물 4

HCID 6228DimethylformamideHCID 69412-Iodobenzoic acidHCID 11430Potassium CarbonateHCID 5207211,3-Dimethyl-1H-pyrazol-5-amine

생성물 1

HCID 615796N-(1,3-Dimethyl-5-pyrazolyl)anthranilic acid수율 44.7%

시약·촉매·용매 2

HCID 8895Cupric acetate촉매HCID 176Acetic Acid용매

실험 절차

A mixture of 2-iodobenzoic acid (14.9 g, 0.06 mol), 5-amino-1,3-dimethylpyrazole (6.7 g, 0.06 mol), DMF (125 ml), Cu(OAc)2 (0,4 g) and K2CO3 (8.28 g, 0.06 mol) was refluxed overnight. The reaction mixture was poured into ice-water (500 ml) and then was acidified with acetic acid to a pH of about 5. The solid which formed was collected by filtration, washed with water (100 ml) and dried. The solid was dissolved in hot CHCl3 (300 ml), filtered, dried over MgSO4 and evaporated to about 20 ml. Hexane (50 ml) was added and then the product was collected by filtration, washed with hexane (30 ml) and dried to afford 6.2 g of N-(1,3-dimethyl-pyrazol-5-yl)anthranilic acid, m.p. 210°-211° C.

후처리

  1. temperaturewas refluxed overnight
  2. customThe solid which formed
  3. filtrationwas collected by filtration
  4. washwashed with water (100 ml)
  5. customdried
  6. dissolutionThe solid was dissolved in hot CHCl3 (300 ml)
  7. filtrationfiltered
  8. dry with materialdried over MgSO4
  9. customevaporated to about 20 ml
  10. additionHexane (50 ml) was added
  11. filtrationthe product was collected by filtration
  12. washwashed with hexane (30 ml)
  13. customdried

출처 및 근거

ORD 기록
ord-9c9551a600524f88842724108d416682
출처 데이터셋
uspto-grants-1997_03
특허 번호
US05614530

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