HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59851270, compound → HCID 59851088, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59851270 | HCID 59851270 | — |
| Reactant | HCID 59851365 | HCID 59851365 | — |
| Product | HCID 59851088 | HCID 59851088 | — |
Reaction Steps
In a manner similar to that described for Method N, 2-(3,4-dimethoxy-phenylamino)-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepine-9-carboxylic acid (I-53) and tert-butyl 4-aminopropylcarbamate were converted to (2-{[2-(3,4-dimethoxy-phenylamino)-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepine-9-carbonyl]-amino}-ethyl)-carbamic acid tert-butyl ester, which was subsequently deprotected (Method K) to give I-72 (30%): HRMS Calcd. for C24H26N6O4: 463.2093, Found 463.2078.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07459448B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-e1784103fb614c188fcd6ecfe277e544 |
| Source note | uspto-grants-2008_12 |