Benzo-1,3-dioxole-5-methylamine → HCID 77750054, compound

HRID 840711Notes

Reaction equation

HRID 840711 reaction equation
[CH2:1]([NH:3][C:4]([CH:6]1[CH2:10][CH:9]([N:11]2[C:15]3[N:16]=[C:17]([S:30][CH2:31][CH2:32][CH3:33])[N:18]=[C:19]([NH:20][CH:21]4[CH2:23][CH:22]4[C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[C:14]=3[N:13]=[N:12]2)[CH:8]([OH:34])[CH:7]1[OH:35])=[O:5])[CH3:2].[O:36]1[C:40]2[CH:41]=[CH:42]C(CN)=[CH:44][C:39]=2[O:38][CH2:37]1>>[O:36]1[C:40]2[CH:41]=[CH:42][C:2]([CH2:1][NH:3][C:4]([CH:6]3[CH2:10][CH:9]([N:11]4[C:15]5[N:16]=[C:17]([S:30][CH2:31][CH2:32][CH3:33])[N:18]=[C:19]([NH:20][CH:21]6[CH2:23][CH:22]6[C:24]6[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=6)[C:14]=5[N:13]=[N:12]4)[CH:8]([OH:34])[CH:7]3[OH:35])=[O:5])=[CH:44][C:39]=2[O:38][CH2:37]1

Participants

3

Reactant 2

HCID 75799Benzo-1,3-dioxole-5-methylamineHCID 77750217HCID 77750217, compound

Product 1

HCID 77750054HCID 77750054, compound

Procedure

The subtitle compound was prepared according to the method of example 39 step a) using the product of example 1, step c) and 2H-1,3-benzodioxol-5-ylmethylamine.

Sources & evidence

ORD record
ord-3f65074e55e648a380a6cfcab3966b18
Source dataset
uspto-grants-2002_04
Patent number
US06369064B1

Reaction notes

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