HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → HCID 18351249, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Benzoylacetonitrile | HCID 64799 | — |
| Reactant | HCID 18351257 | HCID 18351257 | — |
| Product | HCID 18351249 | HCID 18351249 | — |
Reaction Steps
Using the procedures in Examples 7 and 8, substituting p-fluorobenzoyl acetonitrile for benzoyl acetonitrile, 2-amino-3-(4-fluorobenzoyl)-4,5,6,7-tetrahydrothieno(2,3 -c)pyridine was prepared. This compound was reacted with benzyloxycarbonyl chloride to yield the title compound as a solid (mp 90-92° C). 1H NMR (CDCl3) 1.96 (m, 2H); 3.45 (m, 2H); 4.45 (s, 2H); 5.15 (s, 2H); 6.71 (bs, 2H); 7.05-7.52 (m, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323214B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-b657fda90bca4a3387f86973185e67d2 |
| Source note | uspto-grants-2001_11 |