5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine → HCID 178434784, compound

HRID 1980699Notes

Reaction equation

HRID 1980699 reaction equation
CO[C:3]1[C:7](OC)=[N:6][S:5](=[O:11])(=[O:10])[N:4]=1.[CH3:12][C:13]1[C:14]([CH2:18][S:19][CH2:20][CH2:21][NH2:22])=[N:15][O:16][N:17]=1.[CH3:23][N:24]([CH2:26][C:27]1[O:31][C:30]([CH2:32][S:33][CH2:34][CH2:35][NH2:36])=[CH:29][CH:28]=1)[CH3:25]>>[CH3:25][N:24]([CH2:26][C:27]1[O:31][C:30]([CH2:32][S:33][CH2:34][CH2:35][NH:36][C:7]2[C:3]([NH:22][CH2:21][CH2:20][S:19][CH2:18][C:14]3[C:13]([CH3:12])=[N:17][O:16][N:15]=3)=[N:4][S:5](=[O:10])(=[O:11])[N:6]=2)=[CH:29][CH:28]=1)[CH3:23]

Participants

4

Reactant 3

HCID 1622035-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamineHCID 122305383,4-Dimethoxy-1,2,5-thiadiazole 1,1-dioxideHCID 131028982-[(4-Methyl-1,2,5-oxadiazol-3-yl)methylthio]ethylamine

Product 1

HCID 178434784HCID 178434784, compound

Procedure

When a methanolic solution of 3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide is treated with 2-[(4-methyl-1,2,5-oxadiazol-3-yl)methylthio]ethylamine [prepared in Example 58, Step B] and 2-[(5-dimethylaminomethyl-2-furyl)methylthio]ethylamine, the title compound is thereby produced.

Sources & evidence

ORD record
ord-70ad8a52a1374664b49d012c8379599f
Source dataset
uspto-grants-1985_04
Patent number
US04510309

Reaction notes

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