HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 11042299, compound → HCID 136365981, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 11042299 | HCID 11042299 | — |
| Reactant | tert-butyl N-(2-(aminooxy)ethyl)carbamate | HCID 15610443 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 136365981 | HCID 136365981 | 89% |
Reaction Steps
tert-Butyl 2-[[[phenyl(1H-pyrrolo[2,3-c]pyridin-3-yl)methylene]amino]oxy]ethylcarbamate (429.2 mg, 89%) was prepared as a white foam using phenyl(1H-pyrrolo[2,3-c]pyridin-3-yl)methanone (Reference Example 8) and tert-butyl[2-(aminooxy)ethyl]carbamate following the procedure described for Example 104: Rf 0.42 (90:10 methylene chloride/methanol); 1H NMR (300 MHz, CD3OD) δ1.38-1.39 (9H, s), 3.40-3.44 (2H, m), 3.17-3.20 (1H, t, J=5.7 Hz), 3.26-3.28 (1H, t, J=5.3 Hz), 6.50-6.80 (1H, m), 7.30-7.50 (5H, m), 7.86-8.32 (2H, m), 8.76 (1H, s); ESI MS m/z 381 [C21H24N4O3+H]+; HPLC (Method A) 96.8% (AUC), tR=17.7 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07608627B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-16a7c9aa69374ce1899b9d2bb489c76b |
| Source note | uspto-grants-2009_10 |