HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 22449604, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | HCID 15923534 | HCID 15923534 | — |
| Product | HCID 22449604 | HCID 22449604 | 64.3% |
Reaction Steps
Using the method similar to that in Example 61 and cyanogen bromide (657 mg, 6.20 mmol) instead of benzyl bromide and starting from 2,4-dioxo-1-[4-(4-diphenylmethoxypiperidino)butyl]-1,2,3,4-tetrahydroquinazoline (2.50 g, 5.17 mmol) obtained in Example 2, the title compound (1.69 g, 64%) was synthesized. Recrystallization from ethyl acetate yielded a colorless crystal having a melting point of 106 to 107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06407116B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-070d3f8d17b64aea92137391e339b3c5 |
| Source note | uspto-grants-2002_06 |