HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58465801, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methyl-2-pyrrolecarboxylic acid | HCID 81453 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 67438051 | HCID 67438051 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58465801 | HCID 58465801 | — |
Reaction Steps
To a vial containing N-methylpyrrole-2-carboxylic acid (0.025 g, 0.2 mmol) was added HATU (0.076 g, 0.2 mmol), DCM (2 mL), and triethylamine (0.112 mL, 0.8 mmol). The solution was stirred at rt for 30 min then ethyl 2,3,4,5-tetrahydro-1H-pyrrolo[1,2-a][1,4]diazepine-8-carboxylate 2,2,2-trifluoroacetate (0.0644 g, 0.2 mmol) in DMF (0.5 mL) was added. The mixture was stirred at rt for 2 h. The reaction was quenched by addition of DCM (1 mL), sat. NaHCO3 solution (0.5 mL), and water (1 mL). After separation, the aqueous layer was extracted with DCE (2×3 mL). The combined organic layers were concentrated to give crude ethyl 2-(1-methyl-1H-pyrrole-2-carbonyl)-2,3,4,5-tetrahydro-1H-pyrrolo[1,2-a][1,4]diazepine-8-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946223B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-edf14c3a555f434fa81d877a44a71865 |
| Source note | uspto-grants-2015_02 |