HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-((1S,2S,4S)-Bicyclo[2.2.1]hept-5-en-2-yl)acetic acid → HCID 70975747, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-((1S,2S,4S)-Bicyclo[2.2.1]hept-5-en-2-yl)acetic acid | HCID 28063363 | — |
| Reactant | HCID 70976322 | HCID 70976322 | — |
| Product | HCID 70975747 | HCID 70975747 | — |
Reaction Steps
The product from Example 14B and 2-((1S,2S,4S)-bicyclo[2.2.1]hept-5-en-2-yl)acetic acid was processed using a method similar to that described in Example 10C to afford the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.31 (s, 1H), 8.38-8.40 (m, 1H), 7.89-8.05 (m, 2H), 7.72 (d, J=5.1 Hz, 1H), 7.62-7.65 (m, 1H), 7.12 (d, J=5.1 Hz, 1H), 6.22 (dd, J=5.7, 3.0 Hz, 1H), 6.06 (dd, J=5.7, 2.8 Hz, 1H), 2.88-2.90 (m, 1H), 2.77-2.79 (m, 1H), 2.42-2.52 (m, 1H), 2.10 (s, 3H), 2.08 (m, 2H), 1.90 (ddd, J=11.5, 9.1, 3.7 Hz, 1H), 1.33-1.36 (m, 1H), 1.26 (d, J=8.0 Hz, 1H), 0.60 (ddd, J=11.5, 4.3, 2.5 Hz, 1H); MS (APCI) M/Z 392 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859549B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-387f80968921409c8dd2f4367f578709 |
| Source note | uspto-grants-2014_10 |