2-Chloro-6-nitroquinoline → HCID 68632105, compound

HRID 1928838Notes

Reaction equation

HRID 1928838 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-])=O)[CH:8]=2)[N:3]=1.[F:15][C:16]1[CH:17]=[CH:18][CH:19]=[C:20]2[C:24]=1[CH:23]([NH2:25])[CH2:22][CH2:21]2>>[F:15][C:16]1[CH:17]=[CH:18][CH:19]=[C:20]2[C:24]=1[CH:23]([NH:25][C:2]1[CH:11]=[CH:10][C:9]3[C:4](=[CH:5][CH:6]=[C:7]([NH2:12])[CH:8]=3)[N:3]=1)[CH2:22][CH2:21]2

Participants

3

Reactant 2

HCID 109217232-Chloro-6-nitroquinolineHCID 58440160HCID 58440160, compound

Product 1

HCID 68632105HCID 68632105, compound

Procedure

Step C+D: The title compound was prepared in accordance with the general method described in example 2 from 2-chloro-6-nitro-quinoline and rac-7-fluoro-indan-1-ylamine; MS: m/e=294.3 (M+H+).

Sources & evidence

ORD record
ord-b5c7aa41aefd4ee393abba8fc69ab5a1
Source dataset
uspto-grants-2012_05
Patent number
US08183380B2

Reaction notes

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