2-Chloro-6-nitroquinoline → HCID 68638772, compound

HRID 1928804Notes

Reaction equation

HRID 1928804 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]=[C:18]2[C:22](=[CH:23][CH:24]=1)[CH:21]([NH2:25])[CH2:20][CH2:19]2>>[F:15][C:16]1[CH:17]=[C:18]2[C:22](=[CH:23][CH:24]=1)[CH:21]([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)[CH2:20][CH2:19]2

Participants

3

Reactant 2

HCID 109217232-Chloro-6-nitroquinolineHCID 166663285-Fluoro-2,3-dihydro-1H-inden-1-amine

Product 1

HCID 68638772HCID 68638772, compound

Procedure

The title compound was prepared in accordance with the general method described in example 2 from 2-chloro-6-nitro-quinoline and rac-5-fluoro-indan-1-ylamine (CAS no: 148960-33-2); MS: m/e=294.3 (M+H+).

Sources & evidence

ORD record
ord-61e69fcc818e4cddb03fabccb6f69092
Source dataset
uspto-grants-2012_05
Patent number
US08183380B2

Reaction notes

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