HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 66889465, compound → HCID 49854331, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 66889465 | HCID 66889465 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 49854331 | HCID 49854331 | — |
Reaction Steps
Step-2: A solution of benzyl 1-((2-amino-3-carbamoylphenyl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (425 mg, 0.956 mmol) in acetic acid (5 ml) was heated to 80° C. and stirred overnight. The reaction mixture was concentrated, neutralized with aq. NaHCO3 and extracted with DCM. The DCM layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. Purification of the crude product over silica gel column using ethyl acetate/hexane mixture (1:1) as eluent afforded benzyl 1-(4-carbamoyl-1H-benzo[d]imidazol-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate. MS (ES+): m/z 427.2 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513433B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-f4fe45a302064e5bbc24b209af664550 |
| Source note | uspto-grants-2013_08 |