HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565009Generated: October 28, 2026
Guanidine Hydrochloride → HCID 178485130, compound
https://huagongshe.com/reaction/565009
Participants
| Role | Name | HCID | Charge |
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| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | methyl 1-methyl-1H-indole-2-carboxylate | HCID 258548 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178485130 | HCID 178485130 | — |
Reaction Steps
After 8.58 g (89.8 mmol) of guanidine hydrochloride was added to 70 ml of a methanol solution of 4.85 g (89.8 mmol) of sodium methoxide, the mixture was stirred at room temperature. The precipitated sodium chloride was filtered off to obtain the solution. Then 1.70 g (8.97 mmol) of methyl 1-methyl-2-indole-carboxylate was added to the thus obtained solution. Subsequently methanol was distilled off under reduced pressure. The resulting residue was heated at 130° C. for 5 minutes and then allowed to stand at room temperature for an hour. Thereafter water was poured onto the reaction solution and the mixture was extracted three times with ethyl acetate. The combined extracts were washed with water. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was isolated and purified by silica gel column chromatography to give the desired 1-methyl-2-indoloylguanidine. The compound was dissolved in chloroform and treated with hydrogen chloride/ether. Thus 0.70 g (30.8%) of 1-methyl-2-indoloylguanidine hydrochloride was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169107A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-ec4ad3f2feea497a85ae80156211e336 |
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| Source note | uspto-grants-2001_01 |
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