HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990918Generated: October 30, 2026
N-(2-aminoethyl)acetamide → HCID 20608709, compound
https://huagongshe.com/reaction/1990918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(2-aminoethyl)acetamide | HCID 66082 | — |
| Reactant | HCID 20608730 | HCID 20608730 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 20608709 | HCID 20608709 | 93% |
Reaction Steps
A solution containing (8.1) (85 mg, 0.20 mmol), N-acetylethylene-diamine (201 mg, 1.95 mmol) and DMSO (3 mL) was heated to 100° C. After 1 h the temperature was raised to 130° C. After 3 h the reaction was cooled to room temperature and partitioned between EtOAc and water. The water layer was extracted with EtOAc (2×). The combined EtOAc layers are washed with water, dried over MgSO4, filtered and concentrated. Flash chromatography (SiO2; 1/10 EtOH/CHCl3, Rf 0.25) yielded 73 mg (93%) of a white foamy solid, mp. 196-197° C. 1H NMR (200 MHz, DMSO-d6): δ 1.79 (s, 3H), 3.36 (m, 2H), 3.61 (m, 2H), 5.12 (s, 2H), 6.59 (s, 1H), 6.89-7.09 (m, 3H), 7.20-7.50 (m, 5H), 7.57 (brt, 1H), 8.03 (brt, 1H), 8.39 (m, 2H), 11.81 (br s, 1H); MS (ES): 402.6 (MH+). tR (method A)=3.6 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645754B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-4195a871a5ff4e0e9eef3fbab1bb008b |
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| Source note | uspto-grants-2010_01 |
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