HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 2,6-Diamino-4,5-dihydronicotinic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Cyano-2-diaminomethylene-butyric acid ethyl ester | HCID 12494906 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Diamino-4,5-dihydronicotinic acid ethyl ester | HCID 12494905 | 34% |
Reaction Steps
A tetrahydrofuran (7 mL) solution of 2-(2-cyanoethyl)3,3-diaminopropenoic acid ethyl ester (0.55 g, 3 mmol) described in Production Example 1-1-1 was dropped into a tetrahydrofuran (7 mL) suspension of sodium hydride (208 mg, 5.2 mmol, 60% in oil), which was refluxed while heating and stirring for 19 hours 20 minutes. Following completion of the reaction, the reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then concentrated to obtain the title compound (0.188 g, 1 mmol, 34%) as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829585B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-7b08320711b942fc8911f2316fb40de4 |
| Source note | uspto-grants-2010_11 |