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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289756Generated: October 30, 2026

Sodium hydride → HCID 178451140, compound

https://huagongshe.com/reaction/2289756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 86590049HCID 86590049—
ReactantHCID 178479408HCID 178479408—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178451140HCID 17845114017.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

(±)-cis-2-{[(4-Chloro-1-guanidino-7-isoquinolinyl)sulphonyl]amino}cyclohexanecarboxylic acid hydrochloride ##STR56## Guanidine hydrochloride (325 mg, 3.4 mmol) was added in one portion to a stirred suspension of NaH (89 mg, 80% dispersion by wt in mineral oil, 2.97 mmol) in DME (5 mL) and the mixture was heated at 60° C. under N2 for 30 min. A solution of t-butyl (±)-cis-2-{[(1,4-dichloro-7-isoquinolinyl)sulphonyl]amino}cyclohexanecarboxylate (391 mg, 0.85 mmol) in DME (5 mL) was added and the mixture heated at 90° C. for 6 h. The solvents were evaporated in vacuo, the residue was dissolved with EtOAc, washed with aqueous NH4Cl, dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography upon silica gel using using toluene-i-PrOH-0.880NH3 (100:0:0 to 90:10:0.05) as eluant to give t-butyl (±)-cis-2-{[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]amino}cyclohexanecarboxylate (75 mg, 0.15 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-191e10e301294ea7b007e9fbf88b3148
Source noteuspto-grants-2000_07