HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → HCID 11014769, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | N-[(2-Adamantyloxy)carbonyl]-alpha-methyl-D-tryptophan methyl ester | HCID 14802502 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 11014769 | HCID 11014769 | 90% |
Reaction Steps
To a stirred solution of N-[(2-adamantyloxy)carbonyl]-α-methyl-D-tryptophan methyl ester (1.36 g, 3.3 mmol) in aqueous 1,4-dioxan (1:2) (20 mL) was added an excess of LiOH (0.210 g, 5 mmol) and stirred at room temperature overnight. After removing the solvent in vacuo the residue was chromatographed using 5% MeOH:95% CH2Cl2 then 10% MeOH:90% CH2Cl2 as eluants to yield the acid (0.953 mg, 90%) as a white solid, crystallized from n-hexane, mp 210°-215° C. (EtOAc/n-hexane); IR (film) 1689 cm-1 ; NMR (CDCl3 -D2O), δ1.3-2.2 (14H, m), 1.70 (3H, s), 3.26 (1H, d, J 13.5 Hz), 3.63 (1H, d, 13.5 Hz); 4.77 (1H, br.s), 6.85-7.60 (5H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622983 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-df2cc483421a406196083d872ed8b269 |
| Source note | uspto-grants-1997_04 |