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Carbonic Acid → 2-(((S)-1-(8-chloro-2-(2-fluoro-phenyl)quinolin-3-yl)ethyl)carbamoyl)benzoic acid

HRID 216859
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HRID 216859 반응식
Cl[C:2]1[C:11]([C@@H:12]([N:14]2[C:22](=[O:23])[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:15]2=[O:24])[CH3:13])=[CH:10][C:9]2[C:4](=[C:5]([Cl:25])[CH:6]=[CH:7][CH:8]=2)[N:3]=1.[F:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1B(O)O.C(O)(O)=[O:37].C(#N)C.O>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:25][C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:4]=1[N:3]=[C:2]([C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][C:27]=1[F:26])[C:11]([C@@H:12]([NH:14][C:15]([C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:21]=1[C:22]([OH:23])=[O:37])=[O:24])[CH3:13])=[CH:10]2
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참가 물질

6

반응물 4

HCID 767Carbonic AcidHCID 27343542-Fluorophenylboronic acidHCID 18373917Acetonitrile--water (1/1)HCID 57707774(S)-2-(1-(2,8-dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dione

생성물 1

HCID 577077902-(((S)-1-(8-chloro-2-(2-fluoro-phenyl)quinolin-3-yl)ethyl)carbamoyl)benzoic acid

시약·촉매·용매 1

HCID 178418397
HCID 178418397, 화합물
촉매

반응 조건

온도
85 °C

실험 절차

A mixture of (S)-2-(1-(2,8-dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dione (0.5000 g, 1.347 mmol), 2-fluorobenzeneboronic acid (0.2073 g, 1.482 mmol), tetrakis(triphenylphosphine)palladium (0.07782 g, 0.06735 mmol), and sodium carbonate anhydrous (0.7138 g, 6.735 mmol) in acetonitrile-water (3:1) (12.00 mL, 1.346 mmol) was stirred at 85° C. After 28 h, the mixture was cooled to room temperature. The mixture was concentrated under reduced pressure to remove acetonitrile. The mixture was partitioned between CH2Cl2 (50 mL) and water (50 mL). The aqueous layer (pH 10˜11) was washed with CH2Cl2 (50 mL×2) to remove byproducts. The aqueous layer was treated with 2 N HCl (50 mL) and extracted with CH2Cl2 (50 mL×2). The combined organic layers were washed with water (50 mL×1), brine (50 mL×1), dried over Na2SO4, filtered, and concentrated under reduced pressure to give 2-(((S)-1-(8-chloro-2-(2-fluoro-phenyl)quinolin-3-yl)ethyl)carbamoyl)benzoic acid as a solid: LC-MS (ESI) m/z 448.9 [M+H]+. The crude product was carried on crude without purification for the next step.

후처리

  1. temperaturethe mixture was cooled to room temperature
  2. concentrationThe mixture was concentrated under reduced pressure
  3. customto remove acetonitrile
  4. customThe mixture was partitioned between CH2Cl2 (50 mL) and water (50 mL)
  5. washThe aqueous layer (pH 10˜11) was washed with CH2Cl2 (50 mL×2)
  6. customto remove byproducts
  7. additionThe aqueous layer was treated with 2 N HCl (50 mL)
  8. extractionextracted with CH2Cl2 (50 mL×2)
  9. washThe combined organic layers were washed with water (50 mL×1), brine (50 mL×1)
  10. dry with materialdried over Na2SO4
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-edd1f7e2b1f34b83a1b17b1891bbc41a
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08193199B2

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