3-Amino-9-ethylcarbazole → HCID 86729759, compound

HRID 2272602Notes

Reaction equation

HRID 2272602 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:18])[CH2:11][N:12]([CH3:17])[CH2:13][C:14]([OH:16])=O)=[CH:5][CH:4]=1)#[N:2].[CH2:19]([N:21]1[C:33]2[CH:32]=[CH:31][C:30]([NH2:34])=[CH:29][C:28]=2[C:27]2[C:22]1=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH3:20]>>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([NH:9][C:10](=[O:18])[CH2:11][N:12]([CH3:17])[CH2:13][C:14]([NH:34][C:30]2[CH:31]=[CH:32][C:33]3[N:21]([CH2:19][CH3:20])[C:22]4[C:27]([C:28]=3[CH:29]=2)=[CH:26][CH:25]=[CH:24][CH:23]=4)=[O:16])=[CH:7][CH:8]=1)#[N:2]

Participants

3

Reactant 2

HCID 85883-Amino-9-ethylcarbazoleHCID 43442322HCID 43442322, compound

Product 1

HCID 86729759HCID 86729759, compound

Procedure

Using the compound obtained in Step 1 and 9-ethyl-9H-carbazol-3-amine, and by the reaction and purification in the same manner as in the method described in Step 2 of Example 3, the title compound was obtained.

Workup

  1. customby the reaction and purification in the same manner as in the method

Sources & evidence

ORD record
ord-99a51505ea194a52a2c5499f83162db2
Source dataset
uspto-grants-2015_09
Patent number
US09120776B2

Reaction notes

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