HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonate → HCID 16046965, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonate | HCID 11098384 | — |
| Reactant | (4'-Butyl-biphenyl-3-yl)-hydrazine hydrochloride | HCID 66904838 | — |
| Product | HCID 16046965 | HCID 16046965 | — |
Reaction Steps
The title material is prepared by reacting Trifluoro-methanesulfonic acid 5-oxo-5,6,7,8-tetrahydro-naphthalen-2-yl ester and (4′-Butyl-biphenyl-3-yl)-hydrazine hydrochloride (example 70, step 2) in an analogous manner and similar yield to example 1, step 3 except that purification is accomplished by reverse phase UV triggered HPLC. 1H NMR (400 MHz, d6-DMSO) d 11.63 (s, 1H), 7.78 (m, 2H), 7.58 (m, 4H), 7.46 (s, 1H), 7.33 (d, J=6.7 Hz, 1H), 7.28 (m, 2H), 3.09 (m, 2H), 2.95 (m, 2H), 2.64 (m, 2H), 1.60 (m, 2H), 1.35 (m, 2H), 0.94 (m, 3H); LC/MS calculated for [M+H]+ C27H25F3NO3S: 500.5, found: 500.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153671B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-48cc65cd0d3e4e35a0e2005cf2b59b32 |
| Source note | uspto-grants-2012_04 |