1,3-Propanediamine → HCID 178483804, compound
Reaction equation
NC[CH2:3][CH2:4][NH:5][CH2:6][C:7]1[NH:8][C:9]2[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=2[N:11]=1.ClC[C:18]1[NH:19][C:20]2C=CC=CC=2N=1.NCCCN.CN=C=S.N1C2C=CC=CC=2NC=1CNC[CH2:48][CH2:49][NH:50][C:51]([NH:54][C:55]#[N:56])=[N:52]C>>[N:8]1[C:9]2[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=2[NH:11][C:7]=1[CH2:6][NH:5][CH2:4][CH2:3][NH:52][C:51]([NH:54][C:55]#[N:56])=[N:50][CH2:49][CH2:48][N:19]([CH3:20])[CH3:18]Participants
6
Procedure
Using in the above procedure, 2-[(3-aminopropyl)aminomethyl]benzimidazole prepared by reacting 2-chloromethylbenzimidazole with 1.3-diaminopropane) and methyl isothiocyanate, the product is N-[3-(2-benzimidazolylmethylamino)propyl]-N'-cyano-N"-methylguanidine.
Workup
- customprepared
Sources & evidence
- ORD record
- ord-6c67b2f3e7744a9d81f01eca9f57e4f5
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04024271
Reaction notes
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