Hydrochloric Acid → HCID 178485092, compound

HRID 488113Notes

Reaction equation

HRID 488113 reaction equation
[C:1]1([NH:11][C:12]#[N:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH3:14][NH:15][C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([I:22])[CH:17]=1.[ClH:23]>>[ClH:23].[C:1]1([NH:11][C:12]([N:15]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([I:22])[CH:17]=2)[CH3:14])=[NH:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 11075306Benzenamine, 3-iodo-N-methyl-HCID 12295945HCID 12295945, compound

Product 1

HCID 178485092HCID 178485092, compound

Procedure

N-(1-naphthyl)-N'-(3-iodophenyl)-N'-methyl guanidine HCl was prepared from 1-naphthyl cyanamide and N-methyl-3-iodo aniline.HCl by the method similar to the one described in Example 10.C.

Sources & evidence

ORD record
ord-77050e86c7fd4225acac4da7878f810f
Source dataset
uspto-grants-1994_03
Patent number
US05298657

Reaction notes

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