HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993499Generated: October 30, 2026
2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amine → HCID 68415424, compound
https://huagongshe.com/reaction/1993499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amine | HCID 3513851 | — |
| Reactant | (2S)-1-(Chloroacetyl)-4,4-difluoropyrrolidine-2-carbonitrile | HCID 45081037 | — |
| Reactant | HCID 68412925 | HCID 68412925 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68415424 | HCID 68415424 | — |
Reaction Steps
90 mg (0.3 mmole) of N-(3-nitrobenzyl)adamantane-1,3-diamine and 50 mg (0.24 mmole) of (2S)-1-(chloroacetyl)-4,4-difluoropyrrolidine-2-carbonitrile are dissolved in acetonitrile, to the solution 300 mg (0.75 mmole) of polimer bound 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine (PBEMP) are added. The mixture is sirred at 70° C. for 4 hours, then at room temperature for 20 hours. The scavanger resin is fitered off and the filtrate is evapotared, the residue is purified by column chromatography (chloroform-methanol 6:1). After acidification of the formed oil with ethereal hydrochloride acide the title compound is obtained: 41 mg (29%), m.p.: 226-229° C. 1H-NMR (DMSO-d6): 1.57 (s, 2H), 1.95 (d, 8H), 2.45 (d, 4H), 2.91 (m, 2H), 4.14 (m, 2H), 4.33 (m, 4H), 5.21 (m, 1H), 7.74 (t, 1H), 8.15 (t, 1H), 8.27 (dd, 1H), 8.58 (s, 1H), 9.41 (b, 2H), 9.77 (b, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07652021B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-473d6be12c21426d9579428eb2e94f4e |
|---|
| Source note | uspto-grants-2010_01 |
|---|