2-Chloro-6-nitroquinoline → HCID 68622090, compound

HRID 2246422Notes

Reaction equation

HRID 2246422 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=2)[N:3]=1.[C:15]([O:19][C:20]([N:22]1[CH:27]2[CH2:28][CH2:29][CH2:30][CH:23]1[CH2:24][NH:25][CH2:26]2)=[O:21])([CH3:18])([CH3:17])[CH3:16]>>[C:15]([O:19][C:20]([N:22]1[CH:23]2[CH2:30][CH2:29][CH2:28][CH:27]1[CH2:26][N:25]([C:2]1[CH:11]=[CH:10][C:9]3[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=3)[N:3]=1)[CH2:24]2)=[O:21])([CH3:18])([CH3:16])[CH3:17]

Participants

3

Procedure

Is prepared according to method A from 2-chloro-6-nitroquinoline and 3,9-diaza-bicyclo[3.3.1]nonane-9-carboxylic acid tert-butyl ester.

Workup

  1. customIs prepared

Sources & evidence

ORD record
ord-33c21074a0144c8eaa53c80c13fc78b6
Source dataset
uspto-grants-2010_03
Patent number
US07687517B2

Reaction notes

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