HuagongsheHuagongshe Chemistry Print Report · For research reference only
[(1S,2S,4S)-Bicyclo[2.2.1]hept-5-en-2-yl]acetic acid → HCID 67160315, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [(1S,2S,4S)-Bicyclo[2.2.1]hept-5-en-2-yl]acetic acid | HCID 28063363 | — |
| Reactant | HCID 67160399 | HCID 67160399 | — |
| Product | HCID 67160315 | HCID 67160315 | — |
Reaction Steps
The product of Example 129A and 2-[(1S,2S,4S)-bicyclo[2.2.1]hept-5-en-2-yl]acetic acid were treated using a method similar to that described in Example 17C to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ 11.29 (s, 1H), 8.43-8.37 (m, 1H), 8.05-7.88 (m, 2H), 7.76-7.68 (m, 1H), 7.70-7.61 (m, 2H), 7.48-7.34 (m, 2H), 6.22 (dd, J=5.7, 2.9, 1H), 6.06 (dd, J=5.7, 2.8, 1H), 2.92-2.86 (m, 1H), 2.81-2.75 (m, 1H), 2.42-2.48 (m, buried), 2.19-1.98 (m, 2H), 1.90 (ddd, J=11.6, 9.0, 3.8, 1H), 1.39-1.30 (m, 1H), 1.30-1.22 (m, 1H), 0.60 (ddd, J=11.6, 4.2, 2.6, 1H); MS (APCI+) M/Z 390 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629143B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-c579d68adce84973aceead12dad60adf |
| Source note | uspto-grants-2014_01 |