HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492196Generated: October 29, 2026
Guanidine Hydrochloride → HCID 178513070, compound
https://huagongshe.com/reaction/492196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethylacetate methanol | HCID 21584119 | — |
| Reactant | HCID 86596413 | HCID 86596413 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Product | HCID 178513070 | HCID 178513070 | 59.1% |
Reaction Steps
1.25 g (13.09 mmol) of guanidine hydrochloride are added to a solution of 0.71 mg (13.14 mmol) of sodium methoxide in 10 cm3 of methanol at a temperature in the region of 22° C. under an argon atmosphere. After stirring at a temperature in the region of 22° C. for 2 hours, the solvent is evaporated off under reduced pressure (2.7 kPa). The residue, placed under an argon atmosphere, is taken up in 20 cm3 of a tetrahydrofuran/dichloromethane (1/1 by volume) mixture and then 0.9 g (2.62 mmol) of 3-chlorocarbonyl-1-(quinol-8-yl)-1H-indole hydrochloride, dissolved in 5 cm3 of the same tetrahydrofuran/dichloromethane mixture, is added thereto. After 15 hours at a temperature in the region of 22° C. and then heating at a temperature in the region of 60° C. with stirring for 1.5 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give a residue which is taken up in dichloromethane. The insoluble material is then filtered off and discarded, and the filtrate is concentrated under reduced pressure (2.7 kPa). The residue obtained is taken up in an ethyl acetate/methanol (8/2 by volume) mixture and the resulting precipitate is filtered off. A white solid is obtained, which solid is crystallised under hot conditions from 10 cm3 of ethanol. The crystals formed are filtered off and dried under vacuum (2.7 kPa) to give 0.51 g of 3-guanidinocarbonyl-1-(quinol-8-yl)-1H-indole in the form of white crystals melting at 172° C. Mass spectrum (EI): m/e 329 (M+·), m/e 271.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07531663B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-beb72b2899384b9992b917f4535d7310 |
|---|
| Source note | uspto-grants-2009_05 |
|---|