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Chloroform → N-methoxy-N-methyl-4-nitro-2'-methoxymethoxy-6'-methoxy-biphenyl-2-carboxamide

HRID 1358113
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HRID 1358113 반응식
C([Li])CCC.[CH3:6][O:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14][CH2:15][O:16][CH3:17])[CH:9]=1.[CH3:18][O:19][N:20]([CH3:33])[C:21](=[O:32])[C:22]1[CH:27]=[C:26]([N+:28]([O-:30])=[O:29])[CH:25]=[CH:24][C:23]=1Br.C(Cl)(Cl)Cl>C1COCC1.[Cl-].[Zn+2].[Cl-].[Pd](Cl)Cl.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:18][O:19][N:20]([CH3:33])[C:21]([C:22]1[C:23]([C:9]2[C:8]([O:7][CH3:6])=[CH:13][CH:12]=[CH:11][C:10]=2[O:14][CH2:15][O:16][CH3:17])=[CH:24][CH:25]=[C:26]([N+:28]([O-:30])=[O:29])[CH:27]=1)=[O:32]
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참가 물질

8

반응물 4

HCID 6212ChloroformHCID 5426211-Methoxy-3-(methoxymethoxy)benzeneHCID 18188772N-methoxy-N-methyl-2-bromo-5-nitrobenzamideHCID 178418339Butyllithium

생성물 1

HCID 18189308N-methoxy-N-methyl-4-nitro-2'-methoxymethoxy-6'-methoxy-biphenyl-2-carboxamide수율 88%

시약·촉매·용매 3

HCID 3007855
Zincchloride
촉매
HCID 6102075Dichlorobis(triphenylphosphine)palladium촉매
HCID 8028Tetrahydrofuran용매2회

실험 절차

Butyllithium (8.28 ml. of 2.5M in hexane, 20.69 mmole) was added to a solution of 1-methoxy-3 methoxymethoxy benzene (3.62 g., 21.55 mmole, (T. Kaufman, R. Srivastava, R. Sindelar, J. Med. Chem. 1995, 38, 1437-1445) in. THF (15 mL) at −30° C. The solution was stirred at ambient temperature for 1 hour, cooled to at 0° C. and anhydrous zinc chloride beads (3.5 g, 25.67 mmole) added. The mixture was stirred for 2 hours at 25°. Then a solution of N-methoxy-N-methyl-2-bromo-5-nitrobenzamide (5.00 g, 17.24 mmole) dissolved in THF (20 mL) was added. Bis (triphenylphosphine) palladium dichloride (600 mg.) was added and the solution was stirred at 65° C. for 15 hours. After cooling, chloroform was added and the solution stirred with aqueous KHCO3. The precipitated zinc salts were filtered, the water layer removed and the organic layer dried (Na2SO4), filtered concentrated under reduced pressure and the residuepurified on silica gel eluting with 8% ethyl acetate in CH2Cl2 to provide the titled compound (5.68 g, 88% yield).

후처리

  1. customat −30° C
  2. additionadded
  3. stirringThe mixture was stirred for 2 hours at 25°
  4. additionwas added
  5. stirringthe solution was stirred at 65° C. for 15 hours
  6. temperatureAfter cooling
  7. filtrationThe precipitated zinc salts were filtered
  8. customthe water layer removed
  9. dry with materialthe organic layer dried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-648bf1047d70405d923fd46975cfcfba
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06593480B2

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