HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentylamine → HCID 59553207, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide | HCID 59553095 | — |
| Product | HCID 59553207 | HCID 59553207 | — |
Reaction Steps
Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide (0.1 mmol) and cyclopentylamine (10 mmol) according to conditions described in general procedure C. Compound is produced (25 mg) as a light yellow solid; Mp: 119-120° C.; 1H NMR (300 MHz, CDCl3) δ 1.23-1.38(m, 4H), 1.53-1.88(m, 4H), 3.22-3.25(m, 4H), 3.84-3.86(m, 4H), 4.08-4.15(m, 1H), 5.06(bs, 1H), 6.07(bs, 1H), 6.76(d, J=11.7 Hz, 1H), 7.07(d, J=8.4 Hz, 1H), 7.25-7.31(m, 2H), 7.48-7.58(m, 2H), 7.85-7.98(m, 3H), 8.14(s, 1H), 8.25(s, 1H); MS: 528 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114873B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-8e5a69ddd6524f66887ce517a38f64e8 |
| Source note | uspto-grants-2012_02 |