Propargylamine → 1-Nitro-2-(2-propynylamino)-2-{2-[(5-methylaminomethyl-2-furyl)methylthio]ethylamino}ethylene

HRID 1395380Notes

Reaction equation

HRID 1395380 reaction equation
[N+:1]([CH:4]=[C:5](SC)[NH:6][CH2:7][CH2:8][S:9][CH2:10][C:11]1[O:12][C:13]([CH2:16][NH:17][CH3:18])=[CH:14][CH:15]=1)([O-:3])=[O:2].[CH2:21]([NH2:24])[C:22]#[CH:23]>C(#N)C>[N+:1]([CH:4]=[C:5]([NH:24][CH2:21][C:22]#[CH:23])[NH:6][CH2:7][CH2:8][S:9][CH2:10][C:11]1[O:12][C:13]([CH2:16][NH:17][CH3:18])=[CH:14][CH:15]=1)([O-:3])=[O:2]

Participants

4

Reactant 2

HCID 239041PropargylamineHCID 705383981-Nitro-2-methylthio-2-{2-[(5-methylaminomethyl-2-furyl)methylthio]ethylamino}ethylene

Product 1

HCID 867369881-Nitro-2-(2-propynylamino)-2-{2-[(5-methylaminomethyl-2-furyl)methylthio]ethylamino}ethylene

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

A mixture of 1-nitro-2-methylthio-2-{2-[(5-methylaminomethyl-2-furyl)methylthio]ethylamino}ethylene [prepared according to the procedure described in Belgian Pat. No. 857,388] and propargylamine in acetonitrile is stirred and heated under a positive pressure of nitrogen to give, after workup and chromatography, the title compound.

Workup

  1. customprepared
  2. temperatureheated under a positive pressure of nitrogen
  3. customto give

Sources & evidence

ORD record
ord-28cbf161f2b347a1aec3b99d783a71d6
Source dataset
uspto-grants-1980_05
Patent number
US04203909

Reaction notes

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