1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 21948200, compound

HRID 2215021Notes

Reaction equation

HRID 2215021 reaction equation
N([C:8]1[N:17]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:16]2[N:15]=[C:14]([C:24]([OH:26])=O)[CH:13]=[C:12]([CH3:27])[C:11]=2[C:10](=[O:28])[CH:9]=1)C1C=CC=CC=1.Cl.[CH3:30][NH:31][O:32][CH3:33].[CH:34]1[CH:35]=[CH:36][C:37]2N(O)N=[N:40][C:38]=2[CH:39]=1.CCN=C=NCCCN(C)C>C(Cl)Cl>[NH:17]([C:8]1[N:40]([C:38]2[CH:39]=[CH:34][CH:35]=[CH:36][CH:37]=2)[C:16]2[N:15]=[C:14]([C:24]([N:31]([O:32][CH3:33])[CH3:30])=[O:26])[CH:13]=[C:12]([CH3:27])[C:11]=2[C:10](=[O:28])[CH:9]=1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1

Participants

6

Reactant 4

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 81138Methanamine, N-methoxy-, hydrochloride (1:1)HCID 21948162HCID 21948162, compound

Product 1

HCID 21948200HCID 21948200, compoundYield 59%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

7-anilino-4-methyl-5-oxo-8-phenyl-5,8-dihydro-1,8-naphthyridine-2-carboxylic acid (50 mg, 0.14 mmol), N,O-dimethylhydroxylamine hydrochloride (39 mg, 0.40 mmol), HOBT (28 mg, 0.21 mmol), EDCI (40 mg, 0.21 mmol) were dissolved in CH2Cl2 (3 mL). To this solution was added TEA (78 uL, 0.56 mmol). The reaction was stirred for 1 h and was diluted with CH2Cl2, washed with 0.5N HCl, saturated NaHCO3, and brine. The organic layer was collected, dried over Na2SO4, and concentrated in vacuo. The solid obtained was triturated with Et2O and dried to give 7-anilino-N-methoxy-N,4-dimethyl-5-oxo-8-phenyl-5,8-dihydro-1,8-naphthyridine-2-carboxamide as a light yellow solid (34 mg, 59%): LCMS RT: 2.28 min, MH+: 415.2. This transformation can also be accomplished by coupling the appropriate amine with the corresponding acid chloride.

Workup

  1. washwashed with 0.5N HCl, saturated NaHCO3, and brine
  2. customThe organic layer was collected
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. customThe solid obtained
  6. customwas triturated with Et2O
  7. customdried

Sources & evidence

ORD record
ord-c03f71c3eb02422bbde71b96f80d76a7
Source dataset
uspto-grants-2006_09
Patent number
US07109196B2

Reaction notes

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