Anthranilic Acid → HCID 11689687, compound

HRID 2422576Notes

Reaction equation

HRID 2422576 reaction equation
[C:1]([OH:10])(=O)[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[CH2:11]([NH2:13])[CH3:12].[CH:14](=O)[C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1.Cl[CH2:25][CH2:26][CH2:27]Br.[NH:29]1[CH2:34][CH2:33]C[CH2:31][CH2:30]1>>[CH2:11]([N:13]1[C:1](=[O:10])[C:2]2[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:4]=[C:14]1[C:15]1[CH:20]=[CH:19][C:18]([O:21][CH2:22][CH2:31][CH2:30][N:29]2[CH2:34][CH2:33][CH2:27][CH2:26][CH2:25]2)=[CH:17][CH:16]=1)[CH3:12]

Participants

6

Reactant 5

HCID 227Anthranilic AcidHCID 6341EthylamineHCID 80061-Bromo-3-chloropropaneHCID 8082PiperidineHCID 312444-Methoxybenzaldehyde

Product 1

HCID 11689687HCID 11689687, compound

Procedure

The entitled compound was obtained according to the method of Example 1 but starting from anthranilic acid, ethylamine, 4-anisaldehyde, 1-chloro-3-bromopropane and piperidine.

Workup

  1. customThe entitled compound was obtained

Sources & evidence

ORD record
ord-2540cdb0b1404190be792f2b986ab382
Source dataset
uspto-grants-2011_06
Patent number
US07960394B2

Reaction notes

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