HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid → HCID 178421912, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid | HCID 50994114 | — |
| Reactant | HCID 59280056 | HCID 59280056 | — |
| Product | HCID 178421912 | HCID 178421912 | — |
Reaction Steps
The title compound was prepared from N-(5-chloro-2-methyl-3-nitro-2′-trifluoromethyl-biphenyl-4-yl)-acetamide (as prepared in the previous step) and 1-oxa-2-aza-spiro[4.5]dec-2-ene-3-carboxylic acid (as prepared in Example 1, step B) according to the procedures described in Example 1, steps E through H. 1H-NMR (400 MHz, d6-DMSO) δ: 7.87 (d, J=7.6 Hz, 1H), 7.75 (t, J=7.3 Hz, 1H), 7.66 (t, J=7.7 Hz, 1H), 7.40 (d, J=7.3 Hz, 1H), 7.07 (s, 1H), 3.34 (s, 2H), 2.16 (s, 3H), 1.62-1.83 (m, 6H), 1.31-1.61 (m, 4H). Mass Spectrum (LCMS, ESI pos.): Calcd. for C23H21ClF3N3O: 448.1 (M+H). found: 448.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232409B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-d35b1a66e5fc4810b7b3ee83ede51b2d |
| Source note | uspto-grants-2012_07 |