Trimethyl borate → tert-butyl-[2-(1H-indol-5-yl)propan-2-yloxy]silane;[1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid

HRID 456907Notes

Reaction equation

HRID 456907 reaction equation
[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([C:17]([CH3:25])([CH3:24])[O:18][SiH2:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[CH:14][CH:15]=2)[CH:10]=[CH:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C([N-]C(C)C)(C)C.[Li+].C[O:35][B:36](OC)[O:37]C>O1CCCC1>[C:20]([SiH2:19][O:18][C:17]([CH3:25])([CH3:24])[C:13]1[CH:12]=[C:11]2[C:16](=[CH:15][CH:14]=1)[NH:8][CH:9]=[CH:10]2)([CH3:23])([CH3:21])[CH3:22].[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[C:9]1[B:36]([OH:37])[OH:35])=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

5

Reactant 3

HCID 8470Trimethyl borateHCID 2724682Lithium diisopropylamideHCID 131722897Tert-butyl 5-(2-tert-butylsilyloxypropan-2-yl)indole-1-carboxylate

Product 1

HCID 157380136tert-butyl-[2-(1H-indol-5-yl)propan-2-yloxy]silane;[1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a stirred solution of 5-(tert-Butyl-dimethyl-silanyloxymethyl)-indole-1-carboxylic acid tert-butyl ester (5-3, 38.6 g, 106.7 mmol) in tetrahydrofuran (400 mL) was slowly added at −78° C. a solution of lithium diisopropylamide in tetrahydrofuran (2M, 80.1 mL, 160.1 mmol, 1.5 equiv). The reaction mixture was stirred at the same temperature for 1 hour, treated with trimethylborate, warmed up to ambient temperature, and partitioned between ethyl acetate and 0.5N-HCl. The organic layer was washed with brine, separated, dried (MgSO4) and concentrated in vacuo to give the crude solid. Trituation of the crude product with hexanes followed by filtration and air-drying afforded the desired boronic acid (5-4) as a white powder; 1H NMR (400 MHz, CDCl3) δ 7.96 (d, 1H, J=6.8 Hz), 7.54 (s, 1H), 7.47 (s, 1H), 7.32 (d, 1H, J=6.8 Hz), 7.10 (s, 1H), 4.82 (s, 2H), 1.74 (s, 9H), 0.95 (s, 9H), 0.11 (s, 6H).

Workup

  1. custompartitioned between ethyl acetate and 0.5N-HCl
  2. washThe organic layer was washed with brine
  3. customseparated
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customto give the crude solid
  7. filtrationTrituation of the crude product with hexanes followed by filtration
  8. customair-drying

Sources & evidence

ORD record
ord-38bff08842494b08b610c27244a2da94
Source dataset
uspto-grants-2007_03
Patent number
US07186723B2

Reaction notes

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