HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobutyronitrile → HCID 123768507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | HCID 67256382 | HCID 67256382 | — |
| Reactant | tert-butyl(1-(4-(1-(2-cyanoethyl)-2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutyl)carbamate | HCID 123769430 | — |
| Product | HCID 123768507 | HCID 123768507 | — |
Reaction Steps
Following the procedure for tert-butyl(1-(4-(1-(2-cyanoethyl)-2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutyl)carbamate, tert-butyl 1-(4-(2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutylcarbamate (100 mg, 0.212 mmol) was reacted with 4-bromobutanenitrile (94 mg, 0.636 mmol) to afford the title compound (68 mg. 1H NMR (500 MHz, CDCl3): 7.20-7.32 (10H, m), 5.1 (1H, br), 4.90 (2H, s), 4.11 (2H, m), 2.44-2.50 (6H, m), 2.05-2.13 (3H, m), 1.79-1.84 (1H, m), 1.27-1.36 (9H, br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221838B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-decc73fef42b4aea8e2d9139c3cff375 |
| Source note | uspto-grants-2015_12 |