Nitrogen → 4-Methyl-3-[3-(2,3,4-trihydroxy-phenyl)-acryloylamino]-benzoic acid methyl ester

HRID 383591

반응식

HRID 383591 반응식
N#N.[CH3:3][O:4][C:5](=[O:30])[C:6]1[CH:11]=[CH:10][C:9]([CH3:12])=[C:8]([NH:13][C:14](=[O:29])[CH:15]=[CH:16][C:17]2[CH:22]=[CH:21][C:20]([O:23]C)=[C:19]([O:25]C)[C:18]=2[O:27]C)[CH:7]=1.B(Br)(Br)Br.O>C(Cl)Cl.CO>[CH3:12][C:9]1[CH:10]=[CH:11][C:6]([C:5]([OH:30])=[O:4])=[CH:7][C:8]=1[NH:13][C:14](=[O:29])[CH:15]=[CH:16][C:17]1[CH:22]=[CH:21][C:20]([OH:23])=[C:19]([OH:25])[C:18]=1[OH:27].[CH3:3][O:4][C:5](=[O:30])[C:6]1[CH:11]=[CH:10][C:9]([CH3:12])=[C:8]([NH:13][C:14](=[O:29])[CH:15]=[CH:16][C:17]2[CH:22]=[CH:21][C:20]([OH:23])=[C:19]([OH:25])[C:18]=2[OH:27])[CH:7]=1

참가 물질

8

반응물 4

HCID 947NitrogenHCID 962WaterHCID 25134Boron tribromideHCID 52034944-Methyl-3-[3-(2,3,4-trimethoxy-phenyl)-acryloylamino]-benzoic acid methyl ester

생성물 2

HCID 725705854-Methyl-3-[3-(2,3,4-trihydroxy-phenyl)-acryloylamino]-benzoic acid methyl ester수율 25%HCID 725705884-Methyl-3-[3-(2,3,4-trihydroxy-phenyl)-acryloylamino]-benzoic acid수율 19%

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매3회

반응 조건

온도
-78 °C

실험 절차

(The following reaction is done in an anhydrous N2 atmosphere.) Dissolve anilide (53) (40 mg, 0.10 mmol) in anhydrous DCM (1.3 mL) at −78° C., add dropwise a 1M solution of BBr3 in DCM (830 μL, 0.83 mmol) and stir for additional 30 min at −78° C. After slowly warming up stir the reaction solution for additional 4 h at rt. Cool reaction mixture to 0° C., add dropwise water and DCM under vigorous stirring followed by MeOH to homogenize the mixture. Partition the hydrolized reaction mixture between water and EtOAc, extract the aqu. layer with EtOAc (3×), wash combined organic layer with brine and dry it with Na2SO4. Purify the crude product by preparative RP HPLC (gradient, water/CH3CN 95:5 to 5:95) to obtain 4-Methyl-3-[3-(2,3,4-trihydroxy-phenyl)-acryloylamino]-benzoic acid (54) (6.5 mg, 19%) as an yellowish solid and 4-Methyl-3-[3-(2,3,4-trihydroxy-phenyl)-acryloylamino]-benzoic acid methyl ester (55) (9 mg, 25%) as an yellowish solid. 1H NMR (400 MHz, CD3OD) (54): 2.40 (s, 3H); 6.43 (d, 1H, J=8.6 Hz); 6.90 (d, 1H, J=15.6 Hz); 6.97 (d, 1H, J=8.6 Hz); 7.40 (d, 1H, J=8.1 Hz); 7.83 (dd, 1H, J1=8.1 Hz, J2=1.5 Hz); 7.93 (d, 1H, J=15.6 Hz); 8.17 (br.s, 1H); (55): 2.40 (s, 3H); 3.93 (s, 3H); 6.43 (d, 1H, J=8.6 Hz); 6.90 (d, 1H, J=15.7 Hz); 6.97 (d, 1H, J=8.6 Hz); 7.40 (d, 1H, J=8.1 Hz); 7.82 (dd, 1H, J1=7.8 Hz, J2=1.7 Hz); 7.93 (d, 1H, J=15.9 Hz); 8.18 (br.s, 1H).

후처리

  1. custom(The following reaction
  2. temperatureAfter slowly warming up
  3. stirringstir the reaction solution for additional 4 h at rt
  4. temperatureCool
  5. customreaction mixture to 0° C.
  6. stirringunder vigorous stirring
  7. stirringto homogenize the mixture
  8. customPartition the hydrolized reaction mixture between water and EtOAc
  9. extractionextract the aqu
  10. washlayer with EtOAc (3×), wash
  11. dry with materialdry it with Na2SO4
  12. customPurify the crude product by preparative RP HPLC (gradient, water/CH3CN 95:5 to 5:95)

출처 및 근거

ORD 기록
ord-0d47767e40cd44aca33c9da71ec7778b
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08367677B2

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