Methyl 4-chloro-3-nitrobenzoate → HCID 57636250, compound

HRID 1817877Notes

Reaction equation

HRID 1817877 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13].[NH2:15][CH2:16][CH:17]1[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1>>[N+:12]([C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:2]=1[NH:15][CH2:16][CH:17]1[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1)[C:6]([O:8][CH3:9])=[O:7])([O-:14])=[O:13]

Participants

3

Reactant 2

HCID 735797Methyl 4-chloro-3-nitrobenzoateHCID 27732104-Aminomethyltetrahydropyran

Product 1

HCID 57636250HCID 57636250, compound

Procedure

The title compound was prepared according to the procedure described in Step A of Example 5 from methyl 4-chloro-3-nitrobenzoate (Lancaster Synthesis Ltd.) and 4-aminomethyltetrahydropyran (Apollo Scientific Ltd.).

Sources & evidence

ORD record
ord-3695669df4a340f1a987192d6a533525
Source dataset
uspto-grants-2009_10
Patent number
US07598393B2

Reaction notes

Loading…