HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one → N-(11-Oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-thiophene-2-carboxamidine hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one | HCID 10775561 | — |
| Reactant | Thiophene-2-carboximidothioic acid phenyl ester hydrobromide | HCID 66912440 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(11-Oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-thiophene-2-carboxamidine hydrobromide | HCID 178419709 | — |
Reaction Steps
2-Amino-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one (Example 6, 54 mg, 0.24 mmol) was dissolved in methanol (10 mL) and thiophene-2-carboximidothioic acid phenyl ester hydrobromide (79 mg, 0.26 mmol) added. The reaction was stirred at room temperature for 4 hr. The solvent was evaporated and the residue recrystallized from a mixture of methanol and ether to give a yellow solid. The solid was washed several times with ether (84 mg, 0.20, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919328B1 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-8aad96d8e0dc40f2b3f5610d8e1fca31 |
| Source note | uspto-grants-2005_07 |