3-Pyridinemethanamine → HCID 25019063, compound

HRID 2076294Notes

Reaction equation

HRID 2076294 reaction equation
I[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]2.[CH3:13][O:14][C:15]1[CH:23]=[C:22]2[C:18]([CH2:19][CH2:20][CH:21]2[NH2:24])=[CH:17][CH:16]=1.[NH2:25][CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1>>[CH3:13][O:14][C:15]1[CH:23]=[C:22]2[C:18]([CH2:19][CH2:20][CH:21]2[NH:24][C:6]2[CH:5]=[CH:4][C:3]3[C:2]([NH:25][CH2:26][C:27]4[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=4)=[CH:11][CH:10]=[CH:9][C:8]=3[N:7]=2)=[CH:17][CH:16]=1

Participants

4

Reactant 3

HCID 310183-PyridinemethanamineHCID 99204636-Methoxy-1-IndanamineHCID 457894242-Chloro-5-iodoquinoline

Product 1

HCID 25019063HCID 25019063, compound

Procedure

The title compound, MS: m/e=397.1 (M+H+), was prepared in accordance with the general method of example 6 from 5-iodo-2-chloroquinoline, 6-methoxyindan-1-ylamine (CAS 103028-81-5) and 3-(aminomethyl)-pyridine.

Sources & evidence

ORD record
ord-6e71f30c244b4e70b57ad9b72e1fcb1a
Source dataset
uspto-grants-2011_04
Patent number
US07923561B2

Reaction notes

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