HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1,1-dimethylethyl (2-{[({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)amino]carbonyl}-1H-indol-5-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| 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 | 5-(((tert-butoxy)carbonyl)amino)-1H-indole-2-carboxylic acid | HCID 15887147 | — |
| Reactant | 3-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile | HCID 59451392 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,1-dimethylethyl (2-{[({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)amino]carbonyl}-1H-indol-5-yl)carbamate | HCID 59451466 | 60% |
Reaction Steps
HATU (0.064 g, 0.168 mmol) was added to a solution of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.035 g, 0.112 mmol), 5-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-1H-indole-2-carboxylic acid (0.032 g, 0.116 mmol), and DIPEA (0.030 ml, 0.168 mmol) in DMF (1 mL). The mixture was stirred at RT for 1.5 h. Water and EtOAc were added. The organic layer was separated and washed with water and brine, dried over sodium sulfate, and concentrated to give the title compound (0.038 g, 60%) as a colorless oil. 1H NMR (400 MHz, CDCl3): δ ppm 9.67 (s, 1H), 7.75 (s, 1H), 7.17-7.37 (m, 4H), 7.14 (t, 1H), 7.08 (dd, 1H), 6.94-7.02 (m, 2H), 6.80 (m, 1H), 6.60 (s, 1H), 4.69 (d, 2H), 1.52 (m, 9H). MS: m/z 569 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-c43f09bab756402ead9ea1f751d3a151 |
| Source note | uspto-grants-2012_11 |