HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamate → HCID 51002198, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamate | HCID 67130164 | — |
| Reactant | HCID 69812238 | HCID 69812238 | — |
| Product | HCID 51002198 | HCID 51002198 | 51% |
Reaction Steps
Followed the procedure as described in EXAMPLE 1, starting with tert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamate and 2-(1-(tert-butoxycarbonyl)piperidin-3-yl)-5-(tert-butoxycarbonylamino)thiazole-4-carboxylic acid. Obtained the desired product as a white solid (6.4 mg, 51%). 1H NMR (500 MHz, DMSO) δ 9.38 (s, 1H), 8.37 (s, 1H), 8.19 (d, J=5.1 Hz, 1H), 7.28 (s, 2H), 7.11 (d, J=5.1 Hz, 1H), 3.14 (dd, J=28.4, 11.4 Hz, 2H), 2.94 (dd, J=51.3, 24.0 Hz, 4H), 2.65 (dd, J=27.1, 13.0 Hz, 2H), 2.50-2.40 (m, 1H), 2.05 (s, 1H), 1.97-1.56 (m, 5H), 1.47 (d, J=11.2 Hz, 1H), 1.24 (d, J=8.3 Hz, 2H). ESIMS m/z=402.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08435976B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-b8f484f13dc24125923af8edcfc26470 |
| Source note | uspto-grants-2013_05 |