HuagongsheHuagongshe Chemistry Print Report · For research reference only
[(1S,2S,4S)-Bicyclo[2.2.1]hept-5-en-2-yl]acetic acid → HCID 67160083, 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 67161053 | HCID 67161053 | — |
| Product | HCID 67160083 | HCID 67160083 | — |
Reaction Steps
The product of Example 159A 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 ppm 11.26 (s, 1H), 8.37-8.40 (m, 1H), 7.85-7.97 (m, 2H), 7.26-7.32 (m, 1H), 7.20-7.25 (m, 2H), 7.16-7.20 (m, 1H), 6.21 (dd, J=5.7, 2.9 Hz, 1H), 6.05 (dd, J=5.7, 2.9 Hz, 1H), 2.86-2.91 (m, 1H), 2.76-2.81 (m, 1H), 2.41-2.49 (m, 1H), 2.38 (s, 3H), 2.01-2.12 (m, 2H), 2.06 (s, 3H), 1.86-1.93 (m, 1H), 1.33 (dd, J=7.9, 2.5 Hz, 1H), 1.26 (d, J=8.1 Hz, 1H), 0.59 (ddd, J=11.5, 4.3, 2.5 Hz, 1H); MS (APCI+) M/Z 400 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629143B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-ee17f53df4f34b159f93cd219cdbfb2d |
| Source note | uspto-grants-2014_01 |