Potassium Iodide → HCID 21437272, compound

HRID 2397348Notes

Reaction equation

HRID 2397348 reaction equation
[CH2:1]([S:3][C:4]1[C:9]2[C:10]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[CH:21]=3)=[N:11][CH2:12][C:13]3[N:14]([C:15]([CH2:18]Cl)=[N:16][N:17]=3)[C:8]=2[CH:7]=[CH:6][CH:5]=1)[CH3:2].[I-].[K+].[CH2:29]([NH2:32])[CH:30]=[CH2:31]>O1CCCC1>[CH2:1]([S:3][C:4]1[C:9]2[C:10]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[CH:21]=3)=[N:11][CH2:12][C:13]3[N:14]([C:15]([CH2:18][NH:32][CH2:29][CH:30]=[CH2:31])=[N:16][N:17]=3)[C:8]=2[CH:7]=[CH:6][CH:5]=1)[CH3:2]

Participants

5

Reactant 3

HCID 4875Potassium IodideHCID 7853AllylamineHCID 21437245HCID 21437245, compound

Product 1

HCID 21437272HCID 21437272, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

In the manner given in Example 31, 7-(ethylthio)-1-(chloromethyl)-6-(m-chlorophenyl)-4H-s-triazolo[4,3-a]-[1,4] benzodiazepine, potassium iodide and allylamine in tetrahydrofuran are reacted to give 7-(ethylthio)-1-[(allylamino)methyl]-6-(m-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]-benzodiazepine.

Workup

  1. customare reacted

Sources & evidence

ORD record
ord-ad35a53e85374a2dab2df4c8eaf11a0a
Source dataset
uspto-grants-1977_05
Patent number
US04021441

Reaction notes

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