3-(Methylthio)propylamine → HCID 44219079, compound

HRID 1671550Notes

Reaction equation

HRID 1671550 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.[CH3:25][S:26][CH2:27][CH2:28][CH2:29][NH2:30]>>[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:30][CH2:29][CH2:28][CH2:27][S:26][CH3:25])=[CH:11][CH:10]=[CH:9][C:8]=3[N:7]=2)=[CH:17][CH:16]=1

Participants

4

Reactant 3

HCID 777433-(Methylthio)propylamineHCID 99204636-Methoxy-1-IndanamineHCID 457894242-Chloro-5-iodoquinoline

Product 1

HCID 44219079HCID 44219079, compound

Procedure

The title compound, MS: m/e=394.3 (M+H+), was prepared in accordance with the general method of example 1 from 5-iodo-2-chloroquinoline, 6-methoxyindan-1-ylamine (CAS 103028-81-5) and 3-(methylthio)propylamine.

Sources & evidence

ORD record
ord-1901b1c1c40d4fb59d007d03d74a666c
Source dataset
uspto-grants-2011_08
Patent number
US07994324B2

Reaction notes

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