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Triethylamine → HCID 21034913, 화합물

HRID 1833117
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HRID 1833117 반응식
[CH:1]([O:4][C:5]1[CH:6]=[C:7]([CH2:11][C:12](O)=O)[CH:8]=[CH:9][CH:10]=1)([CH3:3])[CH3:2].Cl.[CH2:16]([O:18][C:19](=[O:33])[CH:20]([CH2:31][NH2:32])[C:21]1[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[C:23]([O:29][CH3:30])[CH:22]=1)[CH3:17].C(N(CC)CC)C.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.P(Cl)(Cl)(Cl)(Cl)Cl.[S]>C(Cl)Cl.C(O)C>[CH2:16]([O:18][C:19]([C:20]1[C:21]2[C:26](=[CH:25][C:24]([O:27][CH3:28])=[C:23]([O:29][CH3:30])[CH:22]=2)[C:12]([CH2:11][C:7]2[CH:8]=[CH:9][CH:10]=[C:5]([O:4][CH:1]([CH3:2])[CH3:3])[CH:6]=2)=[N:32][CH:31]=1)=[O:33])[CH3:17]
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참가 물질

9

반응물 6

HCID 8471TriethylamineHCID 24819Phosphorus pentachlorideHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 5362487SulfurHCID 166389242-(3-(Propan-2-yloxy)phenyl)acetic acidHCID 69551005Ethyl 3-amino-2-(3,4-dimethoxyphenyl)propanoate hydrochloride

생성물 1

HCID 21034913HCID 21034913, 화합물수율 55%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6344Dichloromethane용매2회

실험 절차

To a mixture of 3-isopropoxyphenyl acetic acid (3.79 g, 19.54 mmol) and α-aminomethyl-3,4-dimethoxybenzene-acetic acid ethyl ester hydrochloride (5.656 g, 19.54 mmol) in 150 ml of methylene chloride was added triethylamine (5.44 ml, 2.0 eq) and HBTU (8.15 g, 21.50 mmol). The mixture was stirred at room temperature overnight and then extracted with 3N hydrochloric acid and methylene chloride. The organic layer was washed with water and sodium bicarbonate solution. After the evaporation of solvents, an oil was obtained (10.20 g). This oil (10.2 g) was dissolved in 100 ml of methylene chloride. The solution was cooled in an ice bath and then phosphorus pentachloride (10.0 g, 47.96 mmol) was added. The mixture was stirred at room temperature overnight and then poured into ice. The mixture was extracted with methylene chloride. The organic layer was washed with concentrated sodium bicarbonate solution and then dried. After the evaporation of solvents, an oil was obtained. This oil (8.81 g, 21.43 mmol) was mixed with sulfur (755 mg, 23.6 mmol) and the mixture was put into an oil bath preheated to 165° C. and stirred at this temperature for 20 minutes. Then ethanol (100 ml) was added and the mixture was filtered. The filtrate was evaporated and the residue was suspended into ethyl acetate. The solid was removed by filtration and the filtrate was washed with sodium bicarbonate solution. After the evaporation of solvents, the residue was purified through a flash column chromatography using ethyl acetate and hexane (2/1 ratio) to give 1-(3-isopropoxybenzyl)-6,7-dimethoxyisoquinoline-4-carboxylic acid ethyl ester (4.40 g, 55% for 3 steps).

후처리

  1. extractionextracted with 3N hydrochloric acid and methylene chloride
  2. washThe organic layer was washed with water and sodium bicarbonate solution
  3. customAfter the evaporation of solvents
  4. customan oil was obtained (10.20 g)
  5. temperatureThe solution was cooled in an ice bath
  6. stirringThe mixture was stirred at room temperature overnight
  7. additionpoured into ice
  8. extractionThe mixture was extracted with methylene chloride
  9. washThe organic layer was washed with concentrated sodium bicarbonate solution
  10. customdried
  11. customAfter the evaporation of solvents
  12. customan oil was obtained
  13. customthe mixture was put into an oil bath
  14. custompreheated to 165° C.
  15. stirringstirred at this temperature for 20 minutes
  16. filtrationthe mixture was filtered
  17. customThe filtrate was evaporated
  18. customThe solid was removed by filtration
  19. washthe filtrate was washed with sodium bicarbonate solution
  20. customAfter the evaporation of solvents
  21. customthe residue was purified through a flash column chromatography

출처 및 근거

ORD 기록
ord-d8601c4a5e1342e1b59099eb9b0ca927
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067529B2

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