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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770253Generated: October 25, 2026

1-Adamantylcyanamide → N-(Adamantan-1-yl)-N'-(2-iodophenyl)guanidine HCl

https://huagongshe.com/reaction/1770253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AdamantylcyanamideHCID 12435846—
Reactanto-Iodoaniline hydrochlorideHCID 15621116—
ProductN-(Adamantan-1-yl)-N'-(2-iodophenyl)guanidine HClHCID 17847930721%

Reaction Steps

Adamantan-1-ylcyanamide (299 mg, 1.70 mmol) and o-iodoaniline hydrochloride (433 mg 1.70 mmol) were finely ground together and heated at 200° for 10 min. The resultant black glassy solid was pulverized, and recrystallized 5 times from EtOH/Et2O. The resultant faintly blue needles (80 mg) were dissolved in 4 ml EtOH, and passed through a short (<1 cm) column packed from bottom to top with Celite, charcoal, activated alumina, and sand. The colorless eluate was then diluted with 5ml Et2O, and allowed to stand in an Et2O diffusion chamber overnight. The white needles were collected by suction filtration, 40 mg, mp 274°-275° C. Addition of another 5 ml Et2O yielded a second crop (31 mg) of identical material. Combined yield: 21%. 1H (CD3OD) 1.779 (s, 6H), 2.090 (s, 6H), 2.164 (s, 3H), 7.168 (t, 1 H, J=8.1 Hz), 7.388 (d, 1H, J=9.1 Hz), 7.503 (t, 1H, J=7.8 Hz), 8.004 (d, 1H, J=7.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385946
Source datasetuspto-grants-1995_01
ORD IDord-e25f98daafb349fd8b10e200f22ef996
Source noteuspto-grants-1995_01