HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2R)-3-aminopropane-1,2-diol → HCID 69482110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2R)-3-aminopropane-1,2-diol | HCID 6994409 | — |
| Reactant | Ethyl 7-[(4-Fluorophenyl)methyl]-4-hydroxy-1-methyl-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate | HCID 54730000 | — |
| Product | HCID 69482110 | HCID 69482110 | 69.4% |
Reaction Steps
In a similar manner to that described in example 196, from ethyl 7-[(4-fluorophenyl)methyl]-4-hydroxy-1-methyl-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate (50 mg, 0.140 mmol) and (2R)-3-amino-1,2-propanediol (0.03 mL, 0.42 mmol) was prepared N-[(2R)-2,3-dihydroxypropyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-1-methyl-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide (39 mg, 68% yield) as a white solid. 1H NMR (DMSO-d 6)δ 10.44 (br s, 1 H), 8.53 (s, 1 H), 8.01 (s, 1 H), 7.40-7.36 (m, 2 H), 7.15-7.10 (m, 2 H), 5.06 (m, 1 H), 4.77 (m, 1 H), 4.16 (s, 2 H), 3.61-3.55 (m, 4 H), 3.39 (m, 1 H), 3.24 (m, 1 H); MS m/z 402 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691991B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-f39418655ed64ed881a3308eff4c3b65 |
| Source note | uspto-grants-2014_04 |