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3-Bromo-4-[(2-aminoethyl)thiomethyl]pyridine → HCID 178512223, compound

HRID 2058236
Notes
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Reaction equation

HRID 2058236 reaction equation
BrC1C=NC=CC=1CSCCN.C([NH:21][C:22]([NH:35][CH2:36][CH2:37][S:38][CH2:39][C:40]1[C:45]([Br:46])=[CH:44][CH:43]=[CH:42][N:41]=1)=[N:23][CH2:24][CH2:25][S:26][CH2:27][C:28]1[C:33]([Br:34])=[CH:32][CH:31]=[CH:30][N:29]=1)(=O)C1C=CC=CC=1>N1C=CC=CC=1>[Br:46][C:45]1[C:40]([CH2:39][S:38][CH2:37][CH2:36][NH:35][C:22]([NH:23][CH2:24][CH2:25][S:26][CH2:27][C:28]2[C:33]([Br:34])=[CH:32][CH:31]=[CH:30][N:29]=2)=[NH:21])=[N:41][CH:42]=[CH:43][CH:44]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 233499653-Bromo-4-[(2-aminoethyl)thiomethyl]pyridineHCID 54262795N-benzoyl-N',N"-bis-[2-((3-bromo-2-pyridyl)methylthio)ethyl]guanidine

Product 1

HCID 178512223HCID 178512223, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

The reaction of 3-bromo-4-[(2-aminoethyl)thiomethyl]pyridine with N-benzoyl-bis-dimethylthioimidocarbonate in pyridine by the method described in Example 12 yielded N-benzoyl-N',N"-bis-[2-((3-bromo-2-pyridyl)methylthio)ethyl]guanidine which, on acid hydrolysis, yielded the title compound.

Sources & evidence

ORD record
ord-9a57e04c66184fec8eb636c4bbfde326
Source dataset
uspto-grants-1980_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04215125

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes