HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → {[1-(2-pyrrolidin-1-yl-ethyl)-1H-indazol-4-ylcarbamoyl]-methyl}-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | 1-(2-Pyrrolidin-1-YL-ethyl)-1H-indazol-4-ylamine | HCID 11492341 | — |
| Reactant | Ethyldimethylpropylcarbodiimide hydrochloride | HCID 22992078 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {[1-(2-pyrrolidin-1-yl-ethyl)-1H-indazol-4-ylcarbamoyl]-methyl}-carbamic acid tert-butyl ester | HCID 69652714 | — |
Reaction Steps
1-(2-Pyrrolidin-1-yl-ethyl)-1H-indazol-4-ylamine (1.00 g, 4.34 mmol), tert-butoxycarbonylamino-acetic acid (0.836 g, 4.77 mmol), ethyldimethylpropylcarbodiimide hydrochloride (1.00 g, 5.24 mmol), N-hydroxybenzotriazole (0.707 g, 5.24 mmol) and N-methyl morpholine (1.10 g, 10.9 mmol) were dissolved in 30 mL of DMF, and stirred at room temperature for 6 hours. The mixture was concentrated under reduced pressure and the residue purified by flash chromatography to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.41 (s, 9H), 1.62 (m, 4H), 2.44 (m, 4H), 2.86 (t, 2H, J=6.78), 3.86 (d, 2H, J=6.11), 4.47 (t, 2H, J=6.78), 7.08–7.65 (m, 4H), 8.24 (s, 1H), 9.97 (s, 1H); MS (DCI/NH3) m/z 388 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071182B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-0705d34c04cb4ed8b8b6199abebc8b59 |
| Source note | uspto-grants-2006_07 |