HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → 4-Fluoro-3-(4-methoxyphenylmethyl)-1-(beta-D-glucopyranosyl)-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | 4-Fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indole | HCID 67020413 | — |
| Product | 4-Fluoro-3-(4-methoxyphenylmethyl)-1-(beta-D-glucopyranosyl)-indole | HCID 59740084 | — |
Reaction Steps
4-Fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indole obtained in Example 2-(3) and 4-methoxybenzoyl chloride were treated in a manner similar to Example 3 to give the titled compound as a colorless powder. APCI-Mass m/Z 435 (M+NH4)H. 1H-NMR (DMSO-d6) δ 3.21-3.26 (m, 1H), 3.37-3.46 (m, 3H), 3.63-3.68 (m, 2H), 3.70 (s, 3H), 4.02 (s, 2H), 4.53 (t, J=5.4 Hz, 1H), 5.09 (d. J=5.3 Hz, 1H), 5.15 (d. J=5.0 Hz, 1H), 5.20 (d, J=5.9 Hz, 1H), 5.37 (d, J=9.2 Hz, 1H), 6.74 (dd, J=11.2, 7.9 Hz, 1H), 6.83 (d, J=8.5 Hz, 2H), 7.07 (td, J=8.0, 5.2 Hz, 1H), 7.17 (d, J=8.7 Hz, 2H), 7.19 (s, 1H), 7.35 (d, J=8.4 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935674B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-0181170b746d4e4fbc80cb4d834dd0ab |
| Source note | uspto-grants-2011_05 |