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Thionyl Chloride → 7-(2,6-Difluoro-phenoxy)-4-hydroxy-isoquinoline-3-carboxylic acid ethyl ester

HRID 1480963
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HRID 1480963 반응식
C([O:3][C:4](=O)[C:5]1[CH:10]=[CH:9][C:8]([O:11][C:12]2[C:17]([F:18])=[CH:16][CH:15]=[CH:14][C:13]=2[F:19])=[CH:7][C:6]=1[CH2:20][N:21](CC1C=CC(OC)=CC=1OC)[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])C.CCC([O-])(C)C.[K+].S(Cl)(Cl)=O>C1COCC1.C(Cl)Cl>[CH2:26]([O:25][C:23]([C:22]1[N:21]=[CH:20][C:6]2[C:5]([C:4]=1[OH:3])=[CH:10][CH:9]=[C:8]([O:11][C:12]1[C:13]([F:19])=[CH:14][CH:15]=[CH:16][C:17]=1[F:18])[CH:7]=2)=[O:24])[CH3:27]
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참가 물질

6

반응물 3

HCID 24386Thionyl ChlorideHCID 23683543Potassium t-amylateHCID 898130434-(2,6-Difluoro-phenoxy)-2-{[(2,4-dimethoxy-benzyl)-ethoxycarbonylmethyl-amino]-methyl}-benzoic acid ethyl ester

생성물 1

HCID 898130217-(2,6-Difluoro-phenoxy)-4-hydroxy-isoquinoline-3-carboxylic acid ethyl ester수율 64.8%

시약·촉매·용매 2

HCID 6344
Dichloromethane
용매
HCID 8028Tetrahydrofuran용매

실험 절차

To an ice-water bath cooled solution of 4-(2,6-difluoro-phenoxy)-2-{[(2,4-dimethoxy-benzyl)-ethoxycarbonylmethyl-amino]-methyl}-benzoic acid ethyl ester (1.09 g) in THF (10 mL) was added a solution of potassium tert-pentoxide (1.77 mL, 1.7 M in toluene); the mixture was stirred for 30 min at rt after addition; then the mixture was quenched with 2 M HCl (0.9 mL) diluted with EtOAc and water, EtOAc phase was separated and washed with water, diluted NaCl solution and dried over anhydrous sodium sulphate, filtered off, concentrated to give the desired cyclized intermediate. This intermediate was then dissolved in DCM (20 mL) and treated with thionyl chloride (0.15 mL) overnight. Then the reaction mixture was concentrated; the residue was dissolved in EtOAc, washed with water, diluted NaCl solution, then dried over sodium sulphate, filtered, concentrated and the residue was column purified to give the desired product (449 mg). LC MS ESI: 346 (M+1)+.

후처리

  1. additionafter addition
  2. customthen the mixture was quenched with 2 M HCl (0.9 mL)
  3. additiondiluted with EtOAc and water, EtOAc phase
  4. customwas separated
  5. washwashed with water, diluted NaCl solution
  6. dry with materialdried over anhydrous sodium sulphate
  7. filtrationfiltered off
  8. concentrationconcentrated
  9. customto give the
  10. concentrationThen the reaction mixture was concentrated
  11. dissolutionthe residue was dissolved in EtOAc
  12. washwashed with water, diluted NaCl solution
  13. dry with materialdried over sodium sulphate
  14. filtrationfiltered
  15. concentrationconcentrated
  16. custompurified

출처 및 근거

ORD 기록
ord-14eb9bdc54de4091a741ea16bb9a03d5
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409892B2

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