5-Aminoindole → HCID 86627777, compound

HRID 874912Notes

Reaction equation

HRID 874912 reaction equation
[OH:1][P:2]([O:5][P:6]([O:9][P:10]([OH:13])([OH:12])=[O:11])([OH:8])=[O:7])(=[O:4])[OH:3].[N+]([C:17]1[CH:18]=[C:19]2[C:23](=[CH:24][CH:25]=1)[NH:22][CH:21]=[CH:20]2)([O-])=O.[NH2:26]C1C=C2C(=CC=1)NC=C2>>[OH:13][P:10]([O:9][P:6]([O:5][P:2]([OH:4])([OH:3])=[O:1])([OH:8])=[O:7])(=[O:11])[OH:12].[NH2:26][C:21]1[NH:22][C:23]2[C:19]([CH:20]=1)=[CH:18][CH:17]=[CH:25][CH:24]=2

Participants

3

Reactant 2

HCID 788675-AminoindoleHCID 86627778HCID 86627778, compound

Product 1

HCID 86627777HCID 86627777, compound

Procedure

Amino-indole triphosphate was prepared from 5-nitro-indole triphosphate by hydrogenation reaction. The extinction coefficient for 5-amino-indole is 5830 M−1 cm−1 at 270 nm.

Sources & evidence

ORD record
ord-7f106c59365146a5abb9b93241318a33
Source dataset
uspto-grants-2015_03
Patent number
US08981078B2

Reaction notes

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