HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86604861, compound → HCID 87653836, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86604861 | HCID 86604861 | — |
| Reactant | HCID 87653933 | HCID 87653933 | — |
| Product | HCID 87653836 | HCID 87653836 | — |
Reaction Steps
Using the same procedure describe for the synthesis of 39, (R)-2-(3-trifluoromethylbenzenesulfonamido)pent-4-ynoic acid afforded the title compound. 1H NMR (300 MHz, CDCl3): δ 2.05 (s, 1H), 2.65 (m, 2H), 2.85 (s, 3H), 2.96 (s, 3H), 3.35 (m, 2H), 3.96 (t, 6.3 Hz, 1H), 4.32 (t, 5.4 Hz, 1H), 6.86 (t, 5.4 Hz, 1H), 7.68 (t, 7.8 Hz, 1H), 7.82 (d, 7.8 Hz, 1H), 7.97 (s5; 1H), 8.03 (d, 7.8 Hz, 1H), 8.11 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612060B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-42599114354d4e9d8779010d9381d014 |
| Source note | uspto-grants-2009_11 |