HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → HCID 178466868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-Ethoxy-5-(4-ethylpiperazin-1-yl-sulfonyl)benzamidine hydrochloride | HCID 67350956 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178466868 | HCID 178466868 | 74% |
Reaction Steps
The 2-ethoxy-5-(4-ethylpiperazin-1-yl-sulfonyl)benzamidine hydrochloride prepared in the above preparation example 1 was dissolved into ethanol (200 ml), and 85% hydrazine hydrate (5.9 g, 0.1 mol) was slowly dropped into the solution under ice bath. The mixture was stirred for 30 minutes and then at room temperature for 1 hour. Then, the solution was concentrated to dryness, and added with ethyl acetate to perform a recrystallization. The separated crystal was dried under vacuum to obtain 28 g of product with a yield of 74%. 1H NMR (CDCl3, 300 MHz) δ: 1.02 (3H, t), 1.49 (3H, t), 2.39 (2H, q), 2.51 (4H, t), 3.05 (4H, t), 4.18 (2H, q), 7.00 (1H, d), 7.69 (1H, dd), 8.13 (1H, d). ESI-MS m/z 356.3 (M++1, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410098B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-4e13d4efa975423b8ee9d26d921f38f0 |
| Source note | uspto-grants-2013_04 |