HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodobenzoyl chloride → HCID 67195812, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodobenzoyl chloride | HCID 74373 | — |
| Reactant | 4-Chloro-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indole | HCID 67020379 | — |
| Product | HCID 67195812 | HCID 67195812 | — |
Reaction Steps
4-Chloro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-indole obtained in Example 1-(3) and 4-iodobenzoyl chloride were treated in a manner similar to Example 2-(4) to give 4-chloro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-indol-3-yl 4-iodophenyl ketone as a colorless powder. APCI-Mass m/Z 711/713 (M+H). 1H-NMR (DMSO-d6) δ 1.69 (s, 3H), 1.97 (s, 3H), 1.98 (s, 3H), 2.04 (s, 3H), 4.10 (d, J=4.0 Hz, 2H), 4.29 (m, 1H), 5.28 (t, J=9.8 Hz, 1H), 5.53 (t, J=9.6 Hz, 1H), 5.73 (t, J=9.2 Hz, 1H), 6.33 (d, J=9.0 Hz, 1H), 7.29 (d, J=7.7 Hz, 1H), 7.38 (t, J=8.0 Hz, 1H), 7.57 (d, J=8.3 Hz, 2H), 7.79 (d, J=8.4 Hz, 1H), 7.94 (d, J=8.3 Hz, 2H), 8.17 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935674B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-8d296a11d6c146e9a7482dd58539e139 |
| Source note | uspto-grants-2011_05 |