HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Lcb-2183
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-(Ethoxymethyl)pteridin-4-amine | HCID 10798277 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Lcb-2183 | HCID 135418284 | — |
Reaction Steps
A solution of 30.0 g (0.146 mole) of 4-amino-2-(ethoxymethyl)pteridine in 800 ml of 5% aqueous sodium hydroxide is brought slowly to 75° C. and maintained at this temperature for 2 hours. After cooling, the solution obtained is acidified with acetic acid to pH 6 and is then extracted with chloroform. The organic extracts are dried over sodium sulphate and concentrated to dryness under reduced pressure. The solid residue is recrystallized from ethanol in the presence of Norit. Yld: 19.5 g (65%), m.p.=168°-169° C. The product is identical to that obtained in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05167949 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-fae656b4c2a740e9bfcd541d2a727474 |
| Source note | uspto-grants-1992_12 |