HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-Aminoethyl)piperidine → HCID 59553071, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-Aminoethyl)piperidine | HCID 33944 | — |
| Reactant | 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide | HCID 59553095 | — |
| Product | HCID 59553071 | HCID 59553071 | — |
Reaction Steps
Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide and 2-piperidin-1-yl-ethylamine according to conditions described in general procedure C. Mp: 98-100° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.42 (bs, 6 H), 2.06 (s, 2 H), 2.33 (s, 4 H), 2.55-2.94 (m, 2 H), 3.26 (t, J=4.4 Hz, 4 H), 3.77 (t, J=4.8 Hz, 4 H), 6.20-6.35 (bd, 1H), 6.95 (s, 1H), 7.04 (d, J=12.0 Hz, 1H), 7.26 (d, J=8.4 Hz, 1H), 7.40 (d, J=8.0 Hz, 1H), 7.48 (s, 1H), 7.55-7.61 (m, 3H), 7.81-7.83 (m, 1H), 8.00 (d, J=8.4 Hz, 1H), 8.23 (s, 1H), 10.45 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829560B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-a90d8a0405f0428ca709c2582abe6268 |
| Source note | uspto-grants-2010_11 |