2,7-Difluoro-3,6-bis[(2-methoxyethoxy)methoxy]-9h-xanthen-9-one → HCID 68637794, compound

HRID 2357128Notes

Reaction equation

HRID 2357128 reaction equation
[C:1]([O:5][C:6](=[O:32])[CH2:7][N:8]([C:17]1[CH:22]=[CH:21][C:20](Br)=[CH:19][C:18]=1[O:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[CH2:9][C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])([CH3:4])([CH3:3])[CH3:2].C([Li])(C)(C)C.[F:38][C:39]1[C:52]([O:53][CH2:54][O:55][CH2:56][CH2:57][O:58][CH3:59])=[CH:51][C:50]2[O:49][C:48]3[C:43](=[CH:44][C:45]([F:67])=[C:46]([O:60][CH2:61][O:62][CH2:63][CH2:64][O:65][CH3:66])[CH:47]=3)[C:42](=[O:68])[C:41]=2[CH:40]=1>C1COCC1.CC1CCCO1.C1COCC1>[C:1]([O:5][C:6](=[O:32])[CH2:7][N:8]([C:17]1[CH:22]=[CH:21][C:20]([C:42]2([OH:68])[C:43]3[CH:44]=[C:45]([F:67])[C:46]([O:60][CH2:61][O:62][CH2:63][CH2:64][O:65][CH3:66])=[CH:47][C:48]=3[O:49][C:50]3[C:41]2=[CH:40][C:39]([F:38])=[C:52]([O:53][CH2:54][O:55][CH2:56][CH2:57][O:58][CH3:59])[CH:51]=3)=[CH:19][C:18]=1[O:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[CH2:9][C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])([CH3:4])([CH3:3])[CH3:2]

Participants

6

Reactant 3

HCID 593856782,7-Difluoro-3,6-bis[(2-methoxyethoxy)methoxy]-9h-xanthen-9-oneHCID 90684652[(2-Benzyloxy-4-bromo-phenyl)-tert-butoxycarbonylmethyl-amino]-acetic acid tert-butyl esterHCID 178418306HCID 178418306, compound

Product 1

HCID 68637794HCID 68637794, compoundYield 69.3%

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolventHCID 69253648MeTHF THFSolvent

Conditions

Temperature
-105 °C

Procedure

The bromide 13 (807 mg, 1.59 mmol) was dissolved in 20 mL THF/2-methyltetrahydrofuran (1:1) and cooled to −105° C. in a liquid N2/diethyl ether bath. After stirring at −105° C. for 10 min, 4.5 mL of tert-butyllithium (1.1 M in pentanes) was added dropwise. Stirring was continued for another 15 min. 2,7-difluoro-3,6-bis-(2-methoxy-ethoxymethoxy)-xanthen-9-one 9 (912 mg, 2.07 mmol) dissolved in THF (10 mL) was added dropwise to the reaction mixture. The mixture was stirred at −105° C. for 30 min, the cooling bath removed, and the reaction solution was then stirred for an additional 15 min. The resulting mixture was added to 150 mL NH4Cl(sat) and extracted twice with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo. The crude product was purified by flash column chromatography, eluting with 50% EtOAc in hexane (with 0.1% Et3N) to yield 956 mg (69%) of 14 as a orange-red oil. Rf=0.33 (in 50% EtOAc/hexane); 1H NMR (300 MHz, CDCl3) δ 7.32-7.27 (m, 5H), 6.97 (d, 2H, J=6.98 Hz), 6.86 (m, 3H), 6.72 (m, 2H), 5.30 (s, 4H), 5.05 (s, 2H), 4.02 (s, 4H), 3.85 (m, 4H), 3.56 (m, 4H), 3.36 (s, 6H), 1.38 (s, 18H); 13C NMR (75 MHz, CDCl3) δ 170.5, 150.8, 149.3, 147.6, 145.6, 145.5, 145.4, 145.2, 140.5, 138.4, 136.9, 128.3, 127.7, 127.5, 119.9, 119.8, 119.3, 118.4, 115.2, 114.9, 113.0, 104.9, 94.5, 81.0, 71.4, 70.6, 69.7, 68.1, 58.9, 54.6, 28.0; 19F NMR (282 MHz, CDCl3) δ −139.0 (dd, 2 F); mass spectrum, calculated for C46H55F2NO13 (MH+) 868.4, Found 867.8.

Workup

  1. stirringStirring
  2. waitwas continued for another 15 min
  3. additionwas added dropwise to the reaction mixture
  4. stirringThe mixture was stirred at −105° C. for 30 min
  5. customthe cooling bath removed
  6. stirringthe reaction solution was then stirred for an additional 15 min
  7. additionThe resulting mixture was added to 150 mL NH4Cl(sat)
  8. extractionextracted twice with EtOAc
  9. washThe combined organic layers were washed with brine
  10. dry with materialdried over Na2SO4
  11. concentrationconcentrated in vacuo
  12. customThe crude product was purified by flash column chromatography
  13. washeluting with 50% EtOAc in hexane (with 0.1% Et3N)

Sources & evidence

ORD record
ord-b94982b335c747d8b04236ceb4c88b9f
Source dataset
uspto-grants-2010_07
Patent number
US07759459B2

Reaction notes

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