HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Boc-2,6-diazaspiro(3.3)heptane → HCID 118045022, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Boc-2,6-diazaspiro(3.3)heptane | HCID 40151981 | — |
| Reactant | 6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)nicotinamide | HCID 86702637 | — |
| Product | HCID 118045022 | HCID 118045022 | — |
Reaction Steps
The title compound was prepared in an analogous fashion to that described in Example 33 using 6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)nicotinamide (Stage 48.2) and tert-butyl 2,6-diazaspiro[3.3]heptane-2-carboxylate to afford a white powder. HPLC (Condition 4) tR=4.17 min, UPLC-MS (Condition 3) tR=0.77 min, m/z=461 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ ppm 3.30 (br. s, 2H) 3.63 (s, 4H) 3.75-3.92 (m, 4H) 6.41 (d, J=2.35 Hz, 1H) 7.26-7.35 (m, 2H) 7.77 (br. s, 1H) 7.81-7.89 (m, 2H) 8.05 (d, J=2.35 Hz, 1H) 8.71 (d, J=2.35 Hz, 1H) 10.22 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340537B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-e71e6a36d2f1444f9f2c0be870007e32 |
| Source note | uspto-grants-2016_05 |