Potassium Carbonate → HCID 16116867, compound

HRID 1437955Notes

Reaction equation

HRID 1437955 reaction equation
I[C:2]1[CH:3]=[C:4]([N:8]2[C:16](=[O:17])[C:15]3[CH:14]4[C:18]([CH3:20])([CH3:19])[C:11]([CH3:21])([CH2:12][CH2:13]4)[C:10]=3[N:9]2[CH3:22])[CH:5]=[CH:6][CH:7]=1.[CH3:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1B(O)O.C(=O)([O-])[O-].[K+].[K+]>C(COC)OC.ClCCl.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH3:22][N:9]1[C:10]2[C@@:11]3([CH3:21])[C:18]([CH3:20])([CH3:19])[C@H:14]([CH2:13][CH2:12]3)[C:15]=2[C:16](=[O:17])[N:8]1[C:4]1[CH:3]=[C:2]([C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[CH3:23])[CH:7]=[CH:6][CH:5]=1

Participants

7

Procedure

A mixture of 2-(3-iodo-phenyl)-1,7,8,8-tetramethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (Example 23; 80 mg, 0.2 mmol), 2-methyl-phenyl-boronic acid (40 mg, 0.29 mmol), potassium carbonate (66 mg, 0.47 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (10 mg, 0.014 mmol) in dimethoxyethane (4 mL) was sealed under argon and heated at 80 degrees overnight and then at 90 degrees over the weekend. The reaction mixture was diluted with dichloromethane, filtered through a cotton plug and frit, evaporated, and purified using an Analogix Intelliflash 280 system (Analogix, Inc., Burlington, Wis.) with an RS-12 column, eluting with 0-35% ethyl acetate/hexanes to give (4S,7R)-1,7,8,8-tetramethyl-2-(2′-methyl-biphenyl-3-yl)-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (32 mg, 44%) as a light brown solid. ES(+)-MS (M+H) 373.

Workup

  1. customwas sealed under argon
  2. temperatureheated at 80 degrees overnight
  3. customat 90 degrees
  4. filtrationfiltered through a cotton plug and frit
  5. customevaporated
  6. custompurified
  7. washeluting with 0-35% ethyl acetate/hexanes

Sources & evidence

ORD record
ord-ccf311a895e143eaa297798f15cda36b
Source dataset
uspto-grants-2009_11
Patent number
US07622492B2

Reaction notes

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