Methyl 5-aminofuran-2-carboxylate → HCID 22001723, compound

HRID 324998Notes

Reaction equation

HRID 324998 reaction equation
[CH3:1][N:2]([CH3:19])[CH:3]1[CH2:15][C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[C:11]([C:16]([OH:18])=O)[CH:12]=3)[NH:7][C:6]=2[CH2:5][CH2:4]1.[NH2:20][C:21]1[O:22][C:23]([C:26]([O:28][CH3:29])=[O:27])=[CH:24][CH:25]=1>>[CH3:29][O:28][C:26]([C:23]1[O:22][C:21]([NH:20][C:16]([C:11]2[CH:12]=[C:13]3[C:8](=[CH:9][CH:10]=2)[NH:7][C:6]2[CH2:5][CH2:4][CH:3]([N:2]([CH3:1])[CH3:19])[CH2:15][C:14]3=2)=[O:18])=[CH:25][CH:24]=1)=[O:27]

Participants

3

Reactant 2

HCID 5072225Methyl 5-aminofuran-2-carboxylateHCID 123618113-(Dimethylamino)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxylic acid

Product 1

HCID 22001723HCID 22001723, compoundYield 10%

Procedure

Beginning with 7.4 mg (0.029 mMol) 3-dimethylamino-1,2,3,4-tetrahydro-9H-carbazole-6-carboxylic acid and 2-amino-5-methoxycarbonylfuran, 1.3 mg (10%) of the title compound were recovered.

Sources & evidence

ORD record
ord-7ccc8307d0e64f3f9dfe845c52a06565
Source dataset
uspto-grants-2001_04
Patent number
US06221884B1

Reaction notes

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