2-Aminoindane → HCID 44219239, compound

HRID 1671559Notes

Reaction equation

HRID 1671559 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[CH2:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH2:17][CH:16]1[NH2:24]>>[CH2:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH2:17][CH:16]1[NH:24][C:8]1[CH:7]=[CH:6][C:5]2[C:4]([NH2:1])=[CH:13][CH:12]=[CH:11][C:10]=2[N:9]=1

Participants

3

Reactant 2

HCID 763102-AminoindaneHCID 3192512-Chloro-5-nitroquinoline

Product 1

HCID 44219239HCID 44219239, compound

Procedure

The title compound, MS: m/e=276.0 (M+H+), was prepared in accordance with the general method of example 16 from 5-nitro-2-chloroquinoline and indane-2-ylamine.

Sources & evidence

ORD record
ord-a17db27b3b3c42ae96f93f71b3cc0ab7
Source dataset
uspto-grants-2011_08
Patent number
US07994324B2

Reaction notes

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