HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374168Generated: October 30, 2026
2,2-Diphenylethylamine → HCID 19734493, compound
https://huagongshe.com/reaction/374168
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2-Diphenylethylamine | HCID 77575 | — |
| Reactant | 3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl ester | HCID 10081201 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19734493 | HCID 19734493 | 73.1% |
Reaction Steps
Isopropyl N-cyano-3-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (10 ml), and 2,2-diphenylethylamine (0.58 g, 2.9 mmol) was added. The mixture was stirred at room temperature for 2 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residual concentrate thus obtained was subjected to chromatography on a silica gel column (WAKO GEL C 200, 30 g) eluting with chloroform-methanol (100:1). The eluted fractions were concentrated under reduced pressure to give N-cyano-N'-(2,2-diphenylethyl)-3-pyridinecarboximidamide (0.61 g, 1.9 mmol, yield: 71%) as colorless syrup. Next, to this syrup was added a 5% hydrogen chloride solution in methanol (2.5 ml). The solution was crystallized from methanol-diethyl ether to give N-cyano-N'-(2,2-diphenylethyl)-3-pyridinecarboximidamide hydrochloride as colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166347 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-efef8845698043a5bc294860b14582d5 |
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| Source note | uspto-grants-1992_11 |
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