2-Chloro-6-nitroquinoline → HCID 68913457, compound

HRID 1928801Notes

Reaction equation

HRID 1928801 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.[CH3:15][C:16]1[CH:17]=[CH:18][CH:19]=[C:20]2[C:24]=1[CH:23]([NH2:25])[CH2:22][CH2:21]2>>[CH3:15][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 186278267-Methyl-2,3-dihydro-1H-inden-1-amine

Product 1

HCID 68913457HCID 68913457, 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-7-methyl-indan-1-ylamine (CAS no: 168902-78-1); MS: m/e=290.4 (M+H+).

Sources & evidence

ORD record
ord-b179fd003f9644b5ba601902c99ba7c3
Source dataset
uspto-grants-2012_05
Patent number
US08183380B2

Reaction notes

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