Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 4-Pyridinemethanamine | HCID 77317 | — |
| Product | HCID 14978603 | HCID 14978603 | 76% |
Reaction Steps
Making use of racemic 19 (3.00 g, 16.39 mmol), 4-methylmorpholine (1.66 g, 16.39 mmol), isobutylchloroformate (2.24 g, 16.39 mmol), and 4-aminomethylpyridine (1.77 g, 16.39 mmol) in the mixed carbonic anhydride method, gave 3.40 g (76%) of 8: mp 168°-170° C. (recrystallized from EtOAc); Rf 0.31 (8% MeOH/CHCl3); IR (KBr) 3180, 1650 (br), 1480, 1400, 1340, 780, 740 cm-1 ; 1H NMR (DMSO-d6) δ 1.90 (s, C(O)CH3), 4.32 (d, J=5.7 Hz, CH2), 5.57 (d, J=7.8 Hz, CH), 6.32-6.34 (m, C3H), 6.42-6.43 (m, C4H), 7.19 (d, J=4.9 Hz, C3 'H, C5 'H), 7.64 (s, C5H), 8.46 (d, J=4.9 Hz, C2 'H, C6 'H), 8.64 (d, J=7.8 Hz, NH), 8.84 (t, J=5.7 Hz, NH); 13C NMR (DMSO-d6) 22.27 (C(O)CH3), 41.26 (CH2), 50.99 (CH), 107.74 (C4), 110.54 (C3), 121.87 (C3 ', C5 '), 142.63 (C5), 148.17 (C4 '), 149.35 (C2 ', C6 '), 150.82 (C2), 168.35 (C(O)NH), 169.29 (C(O)CH3) ppm; mass spectrum (FD) 274 (M+ +1). Anal. (C14H15N3O3) C, H, N. ##STR42##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05654301 |
|---|
| Source dataset | uspto-grants-1997_08 |
|---|
| ORD ID | ord-ce766b4a7edc4f17a0c25172583bccef |
|---|
| Source note | uspto-grants-1997_08 |
|---|