HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357610Generated: October 25, 2026
Hydrochloric Acid → HCID 178478845, compound
https://huagongshe.com/reaction/357610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Divinylbenzene-styrene | HCID 174664 | — |
| Reactant | 1,2-Diamino-4,5-dihydro-imidazole hydrochloride | HCID 18937940 | — |
| Reactant | HCID 178513250 | HCID 178513250 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178478845 | HCID 178478845 | — |
Reaction Steps
0.5 ml of 32% hydrochloric acid (Merck, Darmstadt, Germany; p.a.) is added, with stirring, to a mixture of 0.51 g (0.0025 mol) of 4-(N-hydroxyamidino)-2,3-dihydro-1H-inden-1-one oxime, 0.342 g (0.0025 mol) of 1,2-diamino-4,5-dihydro-imidazole hydrochloride [m.p. 245°-246° C.; prepared from the corresponding p-toluenesulfonate salt, see EP 0 327 919, Example 12, by ion exchange on ®Amberlite IRA-400 (anion exchanger based on a styrene/divinylbenzene polymer with quaternary ammonium groups in the Cl- form; Fluka, Buchs, Switzerland)] and 12 ml of isopropanol, and the reaction mixture is stirred at 80°-90° C. for 16 hours. The reaction mixture is filtered while hot and the filtration product is washed with isopropanol and recrystallized from hot water. In that manner there is obtained the title compound, m.p. >245° C., 1H-NMR (D2O): δ=8.08 (d, 1H); 7.72 (d, 1H); 7.56 (t, 1H); 4.14 (t, 2H); 3.81 (t, 2H); 3.3 (m, 2H); 3.15 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05840911 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-baf3b5216d004be2abe28a39dc27158b |
|---|
| Source note | uspto-grants-1998_11 |
|---|