HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 135577946, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | HCID 136364562 | HCID 136364562 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 135577946 | HCID 135577946 | 38% |
Reaction Steps
A crude preparation of dimethyl N-[4-[2-(2-acetylamino-4-diacetylamino-1,6-dihydro-6-oxo-5-pyrimidinyl)ethylamino]benzoyl]-L-glutamate hydrate (prepared on a 3.3 mmol scale but without recrystallization) was dissolved in 1N sodium hydroxide (100 ml) and ethanol (50 ml) containing 2-mercaptoethanol (0.25 ml). The reaction was heated with stirring to 55° for 18 hours and then spin evaporated in vacuo to a small volume. The pH of the ice bath cooled solution was adjusted to pH 4 with hydrochloric acid (12 N) to precipiate the product. Recrystallization from methanol/ether gave 0.52 g (38% of theory) of N-[4-[2-(2,4-diamino-1,6-dihydro-6-oxo-5-pyrimidinyl)ethylamino]benzoyl]-L-glutamic acid, mp 180°-185°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880812 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-90a03abcbb33489895bae764aebf38df |
| Source note | uspto-grants-1989_11 |