HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-(Tetrahydropyran-2-yl)hydroxylamine → HCID 87208942, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-(Tetrahydropyran-2-yl)hydroxylamine | HCID 5142091 | — |
| Reactant | HCID 66932405 | HCID 66932405 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87208942 | HCID 87208942 | — |
Reaction Steps
(E)-3-{1′-[2-(4-Amino-phenyl)-ethyl]-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (108 mg, 0.225 mmol) was suspended in DCM (5 ml). TEA (0.09 ml, 0.67 mmol) was added and the clear solution was treated with NH2OTHP following the procedure described in Example 1, Step B, giving (E)-3-{1′-[2-(4-amino-phenyl)-ethyl]-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide (37 mg) as a yellow solid, which was then dissolved in DCM (3 ml) and treated with 4 M HCl in dioxane (0.1 ml, 0.4 mmol) as described in Example 55, Step D, giving a light yellow solid (28 mg, di-hydrochloride salt).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592444B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-3e5012d0a822461b98e234d3cf80f442 |
| Source note | uspto-grants-2013_11 |