4-Amino-2,2,6,6-tetramethylpiperidine → HCID 57936247, compound

HRID 1434955Notes

Reaction equation

HRID 1434955 reaction equation
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[S:7][CH:8]=[CH:9][CH:10]=1.Cl[C:12]1[N:17]=[C:16](Cl)[C:15]([CH3:19])=[CH:14][N:13]=1.[NH2:20][CH:21]1[CH2:26][C:25]([CH3:28])([CH3:27])[NH:24][C:23]([CH3:30])([CH3:29])[CH2:22]1>>[S:1]1[C:5]([C:14]2[C:15]([CH3:19])=[CH:16][N:17]=[C:12]([NH:20][CH:21]3[CH2:22][C:23]([CH3:30])([CH3:29])[NH:24][C:25]([CH3:28])([CH3:27])[CH2:26]3)[N:13]=2)=[CH:4][CH:3]=[C:2]1[C:6]1[S:7][CH:8]=[CH:9][CH:10]=1

Participants

4

Reactant 3

HCID 375244-Amino-2,2,6,6-tetramethylpiperidineHCID 681202,2'-BithiopheneHCID 74508Pyrimidine, 2,4-dichloro-5-methyl-

Product 1

HCID 57936247HCID 57936247, compound

Procedure

The title compound was prepared analogous to Method A, starting from [2,2′]bithiophenyl, 2,4-dichloro-5-methyl-pyrimidine and 4-amino-2,2,6,6-tetramethylpiperidine.

Sources & evidence

ORD record
ord-421a8b0175854b459484754b29b6bfee
Source dataset
uspto-grants-2009_11
Patent number
US07615562B2

Reaction notes

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