Hydrochloric Acid → HCID 70489857, compound
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:9][C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:20][CH2:21][CH2:22][OH:23])=[CH:16][N+:17]([O-:19])=[O:18])=[CH:7][CH:6]=1)[CH3:3].C(O)(C)C.[ClH:28]>C(O)C>[ClH:28].[CH3:3][N:2]([CH2:4][C:5]1[O:9][C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:20][CH2:21][CH2:22][OH:23])=[CH:16][N+:17]([O-:19])=[O:18])=[CH:7][CH:6]=1)[CH3:1]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
a 20 g sample of N-[2-[[(5-[(dimethylamino)methyl]-2-furanyl)methyl]thio]ethyl]-N'-(2-hydroxyethyl)-2-nitro-1,1-ethenediamine (58 mmoles) was dissolved in 100 ml of ethanol (99-100%) and there were added slowly 25 ml of isopropyl alcohol containing 58 mmoles of hydrochloric acid. The mixture was left under stirring overnight and the solid precipitate was filtered, washed with ethanol and dried to give 18 g of N-[2-[[(5-[(dimethylamino)methyl]-2-furanyl)methyl]thio]ethyl]-N'-(2-hydroxyethyl)-2-nitro-1,1-ethenediamine hydrochloride, in the form of white crystals, soluble in water and methanol, m.p. 119°-122° C.
Workup
- waitThe mixture was left
- filtrationthe solid precipitate was filtered
- washwashed with ethanol
- customdried
Sources & evidence
- ORD record
- ord-f8ad842a36894409942480e49d4e4544
- Source dataset
- uspto-grants-1985_05
- Patent number
- US04515806
Reaction notes
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