Pyridine → N-(5-Chloropyridin-2-yl)-5-methoxy-2-nitrobenzamide

HRID 39347노트

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HRID 39347 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([N+:12]([O-:14])=[O:13])=[C:7]([CH:11]=1)[C:8]([OH:10])=O.[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][N:17]=1.N1C=CC=CC=1.P(Cl)(Cl)(Cl)=O>O.C(#N)C>[N+:12]([C:6]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:11][C:7]=1[C:8]([NH:15][C:16]1[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][N:17]=1)=[O:10])([O-:14])=[O:13]

참가 물질

7

반응물 4

HCID 1049PyridineHCID 24813Phosphorus oxychlorideHCID 661742-Amino-5-chloropyridineHCID 3392095-Methoxy-2-nitrobenzoic acid

생성물 1

HCID 21906618N-(5-Chloropyridin-2-yl)-5-methoxy-2-nitrobenzamide수율 88.2%

시약·촉매·용매 2

HCID 962Water용매HCID 6342Acetonitrile용매

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온도
25 °C

실험 절차

5-Methoxy-2-nitrobenzoic acid (A) (25.0 kg, 1.0 eq.), 2-amino-5-chloropyridine (B) (16.3 kg, 1.0 eq.), and acetonitrile (87.5 kg, 3.5 parts) were charged to a 380 L GLMS reactor. The reaction mixture was adjusted to 22° C. (19-25° C.) and anhydrous pyridine (30.0 kg, 3.0 eq.) was added. The pump and lines were rinsed forward with acetonitrile (22.5 kg, 0.9 parts), and the reactor contents were adjusted to a temperature of 19-22° C. Phosphorous oxychloride (23.3 kg, 1.20 eq.) was charged to the contents of the reactor via a metering pump, while maintaining a temperature of 25° C. (22-28° C.). The metering pump and lines were rinsed forward with acetonitrile (12.5 kg, 0.5 parts), while keeping the temperature at 25° C. (22-28° C.). The reaction mixture normally turned from a slurry to a clear solution after the addition of about ⅓ of the POCl3. At the end of the addition, it became turbid. After complete addition, the reaction mixture was agitated at 25° C. (22-28° C.) for ca. 1 hr, at which time HPLC analysis confirmed reaction completion. The solution was cooled to 15° C. (12-18° C.) and drinking water (156.3 kg, 6.25 parts) was charged slowly while keeping reaction temperature of between 12 and 30° C. The reaction mixture was then adjusted to 22° C. (19-25° C.) and agitated for ca. 5 hrs until exotherm ceased. Formation of a slurry was visually confirmed and the contents of the reactor were filtered onto a pressure nutsche fitted with a filter cloth. The reactor, pump, and lines were washed forward onto the pressure nutsche with two portions of drinking water (62.5 kg, 2.5 parts each). The filtrate had a pH value of 7. The product (41.8 kg) was dried under vacuum with a maximum temperature of water bath (to heat dryer jacket) of 50° C. After ca. 12 hrs, in-process LOD analysis indicated a solvent content of 0.72%. The dry product (C) was discharged (34.4 kg) with 88.2% yield and 99.1% purity by HPLC.

후처리

  1. customwas adjusted to 22° C.
  2. additionwas added
  3. washThe pump and lines were rinsed forward with acetonitrile (22.5 kg, 0.9 parts)
  4. customwere adjusted to a temperature of 19-22° C
  5. washThe metering pump and lines were rinsed forward with acetonitrile (12.5 kg, 0.5 parts)
  6. customat 25° C.
  7. custom(22-28° C.)
  8. additionafter the addition of about ⅓ of the POCl3
  9. additionAt the end of the addition, it
  10. additionAfter complete addition
  11. customreaction completion
  12. temperatureThe solution was cooled to 15° C. (12-18° C.)
  13. additionwas charged slowly
  14. customreaction temperature of between 12 and 30° C
  15. customwas then adjusted to 22° C.
  16. custom(19-25° C.)
  17. stirringagitated for ca. 5 hrs
  18. filtrationthe contents of the reactor were filtered onto a pressure nutsche
  19. customfitted with a filter cloth
  20. washThe reactor, pump, and lines were washed forward onto the pressure nutsche with two portions of drinking water (62.5 kg, 2.5 parts each)
  21. dry with materialThe product (41.8 kg) was dried under vacuum with a maximum temperature of water bath
  22. temperature(to heat dryer jacket) of 50° C
  23. waitAfter ca. 12 hrs

출처 및 근거

ORD 기록
ord-1a960dd9689148a5a1cefd13659246bf
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524907B2

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