HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260758Generated: October 26, 2026
1-Adamantylcyanamide → N-(Adamantan-1-yl)-N'-(2-iodophenyl)guanidine HCl
https://huagongshe.com/reaction/2260758
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Adamantylcyanamide | HCID 12435846 | — |
| Reactant | o-Iodoaniline hydrochloride | HCID 15621116 | — |
| Product | N-(Adamantan-1-yl)-N'-(2-iodophenyl)guanidine HCl | HCID 178479307 | 21% |
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 5 ml 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, 1H, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478863 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-687890e6ec1e4e8d9559c7e33792f4ff |
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| Source note | uspto-grants-1995_12 |
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