Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482702Generated: October 25, 2026

Hydrochloric Acid → N-{amino[(3-chlorophenyl)aminocarbonyl]iminomethyl}-N-methylglycine

https://huagongshe.com/reaction/482702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCreatineHCID 586—
ReactantBenzene, 1-chloro-3-isocyanato-HCID 17968—
ReactantTetrabutylammonium HydroxideHCID 2723671—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-{amino[(3-chlorophenyl)aminocarbonyl]iminomethyl}-N-methylglycineHCID 5402511630%

Reaction Steps

A solution of 9.58 g (0.073 mole) of anhydrous creatine in 96 ml (0.073 mole) of 0.76M tetrabutylammonium hydroxide in methanol was evaporated to an oil in vacuo. The residue was dissolved in 100 ml of DMF. An 11.2 g (0.073 mole) sample of m-chlorophenylisocyanate was added dropwise and the reaction was stirred for two hours. The mixture was poured into 200 ml of water and 73 ml of 1N HCl. The gummy precipitate was induced to crystallize by scratching. The solid was collected and triturated with tetrahydrofuran to give 6.6 g (30% yield) of light yellow solid N-{amino[(3-chlorophenyl)aminocarbonyl]iminomethyl}-N-methylglycine. A hydrochloride salt was prepared from conc. HCl to yield a pink solid, m.p. 228°-234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04575514
Source datasetuspto-grants-1986_03
ORD IDord-388581ef70954789afe2084c405d230e
Source noteuspto-grants-1986_03