Methanol → (R)-8-Fluoro-5-methoxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman

HRID 1684091Notes

Reaction equation

HRID 1684091 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5](OS(C(F)(F)F)(=O)=O)=[C:6]2[C:11]=1[O:10][CH2:9][C@H:8]([N:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15])[CH2:7]2.C1(P(C2C=CC=CC=2)CC(P(C2C=CC=CC=2)C2C=CC=CC=2)C)C=CC=CC=1.C(N(CC)CC)C.[CH3:65][OH:66].CN([CH:70]=[O:71])C>C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:65]([O:71][CH3:70])=[O:66])=[C:6]2[C:11]=1[O:10][CH2:9][C@H:8]([N:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15])[CH2:7]2

Participants

7

Procedure

(R)-8-Fluoro-3-(N-3-pentyl-N-n-propylamino)-5-TRIFLUOROMETHANESULFONYLOXYCHROMAN (1.04 g, 2.43 mmol), palladium(II)acetate (55 mg), 1,2-bis(diphenylphosphino)propane (100 mg) was dissolved in 10 ml DMF. Triethylamine (0.75 ml, 5.38 mmol) and MeOH (1.0 ml, 24.6 mmol) was added under CO atm. via septa. The solution was stirred at +70° C. for 18 hours, and thereafter evaporated to dryness. 100 ml 2M NH3 and 100 ml EtOAc was added and the aqueous phase was extracted with 100 ml EtOAc. The combined organic layers was dried (MgSO4) and evaporated. Flash chromatography on silica with a gradient of Hexane--Hexane:EtOAc, 50:1 gave 0.76 g of (R)-8-fluoro-5-methyloxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman as an uncolored oil. Purity: 94% according to GC.

Workup

  1. customevaporated to dryness
  2. addition100 ml 2M NH3 and 100 ml EtOAc was added
  3. extractionthe aqueous phase was extracted with 100 ml EtOAc
  4. dry with materialThe combined organic layers was dried (MgSO4)
  5. customevaporated

Sources & evidence

ORD record
ord-1329ee7629a141ecaac1950cc5279699
Source dataset
uspto-grants-1997_06
Patent number
US05639772

Reaction notes

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