HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Aminocarbonylamino-5-(4-bromophenyl)pyrrole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trichloroacetyl isocyanate | HCID 76400 | — |
| Reactant | 2-Amino-5-(4-bromophenyl)pyrrole-3-carboxamide | HCID 59285978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Aminocarbonylamino-5-(4-bromophenyl)pyrrole-3-carboxamide | HCID 25005704 | 36% |
Reaction Steps
Trichloroacetyl isocyanate (60 μL, 0.50 mmol) was added dropwise to a solution of 2-amino-5-(4-bromophenyl)pyrrole-3-carboxamide (Reference compound No. 1-1, 0.17 g, 0.60 mmol) in anhydrous tetrahydrofuran (3.0 mL) at −40° C. and the mixture was stirred for 1 hour. Furthermore, ammonia solution 2.0 M in methanol (3.0 mL, 6.0 mmol) was added thereto, and the whole was stirred at room temperature for 3 days. Water (20 mL) was added to the reaction solution, then the precipitated solid was filtered off. The obtained solid was dried under reduced pressure to give the target compound (0.070 g) as a brown solid (Yield 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977371B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-1c7be30331e74cf3ab4d22d2ee4f973f |
| Source note | uspto-grants-2011_07 |