5-Aminoindole → HCID 178478388, compound

HRID 1937387Notes

Reaction equation

HRID 1937387 reaction equation
[Cl:1][C:2]1[N:10]=[CH:9][N:8]=[C:7]2[C:3]=1[NH:4][CH:5]=[N:6]2.[NH2:11][C:12]1[CH:13]=[C:14]2[C:18](=[CH:19][CH:20]=1)[NH:17][CH:16]=[CH:15]2>>[ClH:1].[NH:17]1[C:18]2[C:14](=[CH:13][C:12]([NH:11][C:2]3[N:10]=[CH:9][N:8]=[C:7]4[C:3]=3[N:4]=[CH:5][NH:6]4)=[CH:20][CH:19]=2)[CH:15]=[CH:16]1

Participants

3

Reactant 2

HCID 788675-AminoindoleHCID 53592776-Chloropurine

Product 1

HCID 178478388HCID 178478388, compound

Procedure

Following the procedure described in Example 9, the title compound was prepared from 6-chloropurine and 5-aminoindole (70%). TS-MS: 251 (MH+); anal. RP18-HPLC RT: 2.44 min.

Sources & evidence

ORD record
ord-92df826d80024122805cb4040375bfba
Source dataset
uspto-grants-2002_05
Patent number
US06395733B1

Reaction notes

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