Nitrogen → HCID 136195314, compound

HRID 1479586Notes

Reaction equation

HRID 1479586 reaction equation
C[O:2][C:3]1[CH:17]=[CH:16][C:6]2=[C:7]3[C:12](=[C:13]([NH2:15])[N:14]=[C:5]2[CH:4]=1)[N:11]=[CH:10][CH:9]=[CH:8]3.B(Br)(Br)Br.N#N>C(Cl)Cl>[NH2:15][C:13]1[C:12]2[N:11]=[CH:10][CH:9]=[CH:8][C:7]=2[C:6]2[CH:16]=[CH:17][C:3]([OH:2])=[CH:4][C:5]=2[N:14]=1

Participants

5

Reactant 3

HCID 947NitrogenHCID 25134Boron tribromideHCID 44232400HCID 44232400, compound

Product 1

HCID 136195314HCID 136195314, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 8-methoxybenzo[f][1,7]naphthyridin-5-amine (from Example 10) (1.0 eq.) in DCM (0.04 M) was added BBr3 (2.5 eq.) dropwise under N2 at −20° C. The reaction was allowed to warm to ambient temperature over 30 minutes. The reaction was then stirred overnight. The reaction was quenched with saturated NaHCO3 and extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4 and concentrated en vaccuo to obtain a crude residue. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-20% MeOH/DCM to give 5-aminobenzo[f][1,7]naphthyridin-8-ol as a yellow solid: 1H NMR (acetone-d6): δ 8.90 (dd, 1H), 8.83 (dd, 1H), 8.32 (d, 1H), 7.83 (dd, 1H), 7.11 (br s, 2H), 7.10 (d, 1H), 6.96 (dd, 1H), 5.86 (br s, 1H). LRMS [M+H]=212.1.

Workup

  1. customThe reaction was quenched with saturated NaHCO3
  2. extractionextracted with EtOAc
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated en vaccuo
  6. customto obtain a crude residue
  7. customThe crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO)

Sources & evidence

ORD record
ord-bad96b19ced04dc3a86121f64309438c
Source dataset
uspto-grants-2016_08
Patent number
US09408907B2

Reaction notes

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