HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Methoxide → HCID 21308801, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 21308802 | HCID 21308802 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium methanolate methanol | HCID 23694274 | — |
| Product | HCID 21308801 | HCID 21308801 | — |
Reaction Steps
Compound 49 (1.4 g) was dissolved in methanol to which sodium methoxide-methanol solution was added dropwise to pH 11.0 and stirred at room temperature. The pH was adjusted to 11.0 with fresh sodium methoxide solution several times until the pH was stable (approximately 1 hr). The reaction mixture was acidified with Dowex-H type resin and the resin was removed from the solution by filtration. The solvent was removed from the filtrate under vacuum to give 2-acetamido-1-(N-CBZ-6-aminohexanamido)-1,2-dideoxy-a-D-galactopyranose, 50, as a gum (630 mg). 1H NMR (CDCl3): 1H NMR (CD3OD): 7.35-7.40, s, 5H, C6H5CH2—; 5.78-5.8,m, 1H; 5.12, s, 2H, C6H5CH2; 4.45-3.8, m, 6H; 3.65-3.6, m, 1H; 2.22,s, 3H; NHCOCH3; 1.5-1.7, m, 10H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187762B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-b544a257c29e44d4a70d4f77eb2eeb18 |
| Source note | uspto-grants-2001_02 |