HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → HCID 178493891, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-aminopyrimidine-5-carboxylic Acid | HCID 7020367 | — |
| Reactant | (S)-glycidyl methanesulfonate | HCID 12461090 | — |
| Reactant | HCID 178493879 | HCID 178493879 | — |
| Product | HCID 178493891 | HCID 178493891 | — |
Reaction Steps
Prepared using (S)-glycidyl methanesulfonate (Intermediate H, Step 1) in place of (R)-glycidyl methanesulfonate (Intermediate F, Step 1), and morpholine in place of piperidine in Step 1, and 2-amino-5-pyrimidinecarboxylic acid in place of nicotinic acid in Step 2 (75.0 mg, 71%): HPLC ret. time 0.81 min.; 1H NMR (DMSO-d6+1 drop TFA-d) δ 3.14-3.38 (m, 4H), 3.44-3.52 (m, 2H), 3.69 (app t, J=12.0 Hz, 1H), 3.77/app t, J=12.1 Hz, 1H), 3.90-3.98 (m, 2H), 4.00 (s, 3H), 4.16-4.25 (m, 4H), 4.38-4.44 (m, 1H), 4.46-4.52 (m, 2H), 7.43 (d, J=9.1 Hz, 1H), 7.99 (d, J=9.1 Hz, 1H), 8.97 (s, 2H); mass spectrum m/z 497 ((M+1)+, 8.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895549B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-93865345d3ad43658a2d7c7da1315eea |
| Source note | uspto-grants-2014_11 |