HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667244Generated: October 31, 2026
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 45274609, compound
https://huagongshe.com/reaction/1667244
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-(2-Oxo-3,3-diphenylpiperidin-1-yl)acetic acid | HCID 67359280 | — |
| Reactant | HCID 178506461 | HCID 178506461 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 45274609 | HCID 45274609 | — |
Reaction Steps
N1-((Ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (0.160 g, 0.837 mmol), (Z)-2-(4-chlorophenyl)-N-hydroxyacetimidamide (0.103 g, 0.558 mmol) and 2-(2-oxo-3,3-diphenylpiperidin-1-yl)acetic acid (0.173 g, 0.558 mmol; Example 68E) were stirred together in dichloroethane at room temperature for 2 hours, then heated to 85° C. for 16 hours. The reaction was cooled and concentrated. The residue was dissolved in dichloromethane (3 mL) and washed with water (1 mL). The organic layer was concentrated and the residue was loaded onto a GraceResolv™ 12 g silica gel column (Grace Davison Discovery Sciences) and the product eluted with a gradient of 5% ethyl acetate/hexanes to 35% ethyl acetate/hexanes (Flow=35 mL/minute) over 30 minutes to give the title compound. 1H NMR (300 MHz, CDCl3) δ 7.38-7.15 (m, 14H), 4.82 (s, 2H), 4.06 (s, 2H), 3.53 (t, J=6.5, 2H), 2.73-2.58 (m, 2H), 1.95-1.76 (m, 2H); MS (ESI+) m/z 458.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044069B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-1c4c81e6991d4c6aa662ad907cea2cac |
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| Source note | uspto-grants-2011_10 |
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