HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21877256, compound → HCID 135839319, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21877256 | HCID 21877256 | — |
| Reactant | HCID 21877272 | HCID 21877272 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 135839319 | HCID 135839319 | — |
Reaction Steps
6-(4-Benzyloxy-3-methoxy-phenyl)-3-naphthalen-2-yl-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazole was converted to 6-(4-benzyloxy-3-methoxy-phenyl)-3-naphthalen-2-yl-1H-indazole as described in Example 1(a), step (ix). Rf sm 0.40, p 0.17 (ethyl acetate-hexane 3:7); 1H NMR (CDCl3) δ 8.40 (s, 1H), 8.12 (d, 1H, J=8.5 Hz), 8.10 (dd, 1H, J=1.6, 8.4 Hz), 7.93 (d, 1H, J=8.3 Hz), 7.88 (m, 2H), 7.61 (m, 1H) 7.56 (s, 1H), 7.43 (m, 5H), 7.30 (m, 3H), 7.15 (d, 1H, J=2.0 Hz), 7.08 (dd, 1H, J=2.1, 8.3 Hz), 6.91 (d, 1H, J=8.3 Hz), 5.16 (s, 2H), 3.91 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06891044B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-3560ec4e8cfe4242bba87e24856d50e6 |
| Source note | uspto-grants-2005_05 |