1-(tert-Butoxycarbonyl)-2-pyrroleboronic Acid → tert-Butyl 2-cyano-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate

HRID 2120730Notes

Reaction equation

HRID 2120730 reaction equation
BrC1C=CC2[NH:10][CH:9](C)OC(C)(C)C=2C=1.C(OC(N1C=CC=C1B(O)O)=O)(C)(C)C.[C:30]([O:34][C:35]([N:37]1[C:41]([C:42]2[CH:43]=[CH:44][C:45]3[NH:50][CH:49]([CH3:51])[O:48][C:47]([CH3:53])([CH3:52])[C:46]=3[CH:54]=2)=[CH:40][CH:39]=[CH:38]1)=[O:36])([CH3:33])([CH3:32])[CH3:31].S([O-])([O-])(=O)=O.[NH4+].[NH4+]>C1COCC1.C(OCC)(=O)C.CN(C=O)C>[C:30]([O:34][C:35]([N:37]1[C:41]([C:42]2[CH:43]=[CH:44][C:45]3[NH:50][CH:49]([CH3:51])[O:48][C:47]([CH3:53])([CH3:52])[C:46]=3[CH:54]=2)=[CH:40][CH:39]=[CH:38]1)=[O:36])([CH3:33])([CH3:31])[CH3:32].[C:9]([C:38]1[N:37]([C:35]([O:34][C:30]([CH3:33])([CH3:31])[CH3:32])=[O:36])[C:41]([C:42]2[CH:43]=[CH:44][C:45]3[NH:50][CH:49]([CH3:51])[O:48][C:47]([CH3:53])([CH3:52])[C:46]=3[CH:54]=2)=[CH:40][CH:39]=1)#[N:10]

Participants

9

Reactant 4

HCID 27343211-(tert-Butoxycarbonyl)-2-pyrroleboronic AcidHCID 6097028Ammonium SulfateHCID 234355746-Bromo-2,4,4-trimethyl-2,4-dihydro-1H-benzo[D][1,3]oxazineHCID 54467598tert-Butyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate

Product 2

HCID 23435570tert-Butyl 2-cyano-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylateYield 1.78%HCID 54467598tert-Butyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate

Reagents, catalysts & solvents 3

HCID 6228DimethylformamideSolventHCID 8028TetrahydrofuranSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
-78 °C

Procedure

tert-Butyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate was prepared according to the coupling procedure for Example 17 from 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine and 1-t-butoxycarbonylpyrrol-2-yl boronic acid. To a solution of tert-butyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate (1 g, 2.9 mmol) in anhydrous THF (20 mL) was added at −78° C. under nitrogen chlorosulfonyl isocyanate (0.35 mL, 4.0 mmol). The mixture was kept stirring at −78° C. under nitrogen for 2 hours, treated with anhydrous DMF (5 mL), and allowed to warm to room temperature. Aqueous ammonium sulfate solution (50 mL) and ethyl acetate (100 mL) was added and organic layer was separated, dried (MgSO4), and evaporated. The residue was purified by a silica gel column chromatography (hexane:ethyl acetate/4:1) to afford the title compound as a white solid (0.019 g, 1.78%): 1H-NMR (DMSO-d6) δ 7.48 (d, 1H, J 2.0 Hz), 7.36 (dd, 1H, J=8.3, 2.0 Hz), 7.32 (d, 1H, J=3.6 Hz), 7.14 (d, 1H, J=8.3 Hz), 6.46 (d, 1H, J=4.0 Hz), 5.35 (q, 1H, J=5.2 Hz), 1.58 (d, 3H, J=5.6 Hz), 1.56 (s, 3H), 1.51 (s, 3H), 1.38 (s, 9H); MS (ESI) m/z 366 [M−H]−.

Workup

  1. temperatureto warm to room temperature
  2. customorganic layer was separated
  3. dry with materialdried (MgSO4)
  4. customevaporated
  5. customThe residue was purified by a silica gel column chromatography (hexane:ethyl acetate/4:1)

Sources & evidence

ORD record
ord-334171615adc499ba8220e3442950747
Source dataset
uspto-grants-2004_02
Patent number
US06693103B2

Reaction notes

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