Potassium Iodide → HCID 21437300, compound

HRID 2397318Notes

Reaction equation

HRID 2397318 reaction equation
[I-].[K+].[F:3][C:4]1[CH:5]=[CH:6][C:7]2[N:13]3[C:14]([CH2:17]Cl)=[N:15][N:16]=[C:12]3[CH2:11][N:10]=[C:9]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[Cl:25])[C:8]=2[CH:26]=1.C[NH:28]C1CC1.O1[CH2:36][CH2:35][CH2:34][CH2:33]1>>[F:3][C:4]1[CH:5]=[CH:6][C:7]2[N:13]3[C:14]([CH2:17][NH:28][CH2:33][CH:34]4[CH2:36][CH2:35]4)=[N:15][N:16]=[C:12]3[CH2:11][N:10]=[C:9]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[Cl:25])[C:8]=2[CH:26]=1

Participants

5

Reactant 4

HCID 4875Potassium IodideHCID 8028TetrahydrofuranHCID 11029756N-MethylcyclopropanamineHCID 21437262HCID 21437262, compound

Product 1

HCID 21437300HCID 21437300, compound

Procedure

In the manner given in Example 2, potassium iodide and 8-fluoro-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine in tetrahydrofuran is treated with methylcyclopropylamine to give 8-fluoro-1-[(cyclopropylmethylamino)methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine.

Sources & evidence

ORD record
ord-fb06ad69bc104682bdd06e1c04f33338
Source dataset
uspto-grants-1977_05
Patent number
US04021441

Reaction notes

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