HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289719Generated: November 1, 2026
Guanidine Hydrochloride → HCID 178451238, compound
https://huagongshe.com/reaction/2289719
Participants
| Role | Name | HCID | Charge |
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| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | HCID 18698258 | HCID 18698258 | — |
| Reactant | HCID 178512672 | HCID 178512672 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 178451238 | HCID 178451238 | 40.3% |
Reaction Steps
N-[(4-Chloro-1-guanidino-7-isoquinolinyl)sulphonyl]-N-(3-chlorobenzyl)glycine trifluoroacetate ##STR23## NaH (35 mg, 80% dispersion by wt in mineral oil, 1.16 mmol) was added in one portion to a suspension of guanidine hydrochloride (150 mg, 1.55 mmol) in DME (10 mL) and the mixture was heated at 60° C. under N2 for 30 min. N-[(1,4-Dichloro-7-isoquinolinyl)sulphonyl]-N-(3-chlorobenzyl)glycine t-butyl ester (185 mg, 0.36 mmol) was added and the mixture heated at 90° C. for 5 h. The cooled mixture was diluted with Et2O, washed with water, dried (Na2SO4) and evaporated in vacuo. The residue was dissolved in Et2O and a solution of HCl in Et2O (1 M) was added to give a precipitate. The solvents were evaporated in vacuo, and the white solid triturated with EtOAc and then dried to give N-[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]-N-(3-chlorobenzyl)glycine t-butyl ester hydrochloride (85 mg, 0.145 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06093731 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-e63166ae7aee47ae8c1dd3ad1ad86afb |
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| Source note | uspto-grants-2000_07 |
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