HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(tert-butoxycarbonyl)glycine → 1,1-dimethylethyl {2-[(2-{[({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)amino]carbonyl}-1H-indol-5-yl)amino]-2-oxoethyl}carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Amino-N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-1H-indole-2-carboxamide | HCID 59451399 | — |
| Reactant | BOP chloride | HCID 131720136 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,1-dimethylethyl {2-[(2-{[({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)amino]carbonyl}-1H-indol-5-yl)amino]-2-oxoethyl}carbamate | HCID 86644888 | 80% |
Reaction Steps
BOP chloride (0.085 g, 0.334 mmol) was added to a solution of 6-amino-N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-1H-indole-2-carboxamide (0.065 g, 0.111 mmol), N-{[(1,1-dimethylethyl)oxy]carbonyl}glycine (0.0195 g, 0.111 mmol) and diisopropylethylamine (0.097 mL, 0.557 mmol) in DMF (1 mL). The mixture was stirred at room temperature for 1 hr, then extracted with ethyl acetate and water. The organic layer was washed with water, dried over sodium sulfate and concentrated. The residue was purified by flash chromatography (hexane:ethyl acetate) to give the title compound (0.031 g, 80% pure). ES MS: m/z 624 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-deca4659167e4d0dade99cfbc98c05fc |
| Source note | uspto-grants-2012_11 |