HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 59376011, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-Amino-3-(diethylamino)propan-2-ol | HCID 97749 | — |
| Reactant | HCID 59376005 | HCID 59376005 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59376011 | HCID 59376011 | 81% |
Reaction Steps
A mixture of 2-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (S4) 0.2 g (1.0 mmol), HOBt 0.16 g (1.2 mmol), EDCI 0.24 g (1.2 mmol) and triethylamine 0.2 g (2.0 mmol) in 10 ml DMF was stirred at room temperature for 20 min, then 1-amino-3-(diethylamino)propan-2-ol 0.31 g (2.1 mmol) was added. After stirred at room temperature for 24 hours, the mixture was poured into the ice water and extracted with CH2Cl2. The organic layer separated was washed with water and saturated sodium chloride solution, then dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column, eluted with CH2Cl2/MeOH (3:1), to give 0.26 g (81%) of the titled compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084621B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-66363e614246499fa6294856e88a3cad |
| Source note | uspto-grants-2011_12 |