HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indomethacin → HCID 67388927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indomethacin | HCID 3715 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 67388927 | HCID 67388927 | — |
Reaction Steps
Indomethacin A2 (R3=H, R1a=4-Cl) (1 g, 2.8 mmol) and N-bromosuccinimide (0.539 g, 3.08 mmol) were suspended in tetrachloromethane (50 ml) and kept at room temperature for 12 h. The reaction mixture was heated to boiling and filtered off from succinimide. The solid was washed with hot tetrachloromethane (150 ml). The solvent was evaporated in vacuo. Prepared 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)-acetohypobromoanhydride was boiled in CCl4 (50 ml) for 1.5 h. 2-((2-(Bromomethyl)-1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetic acid 1 h (R1=4-chlorobenzoyl, R3═R4═R5═H, R6═CH3) was prepared and used in further reactions without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481587B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-a3a76a342aa147e59ed7f2fe01ee2f57 |
| Source note | uspto-grants-2013_07 |