HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 123817435, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22034371 | HCID 22034371 | — |
| Product | HCID 123817435 | HCID 123817435 | — |
Reaction Steps
To a stirred solution of sodium hydride (45 mg of 60% dispersion in mineral oil) in dry tetrahydrofuran (10 ml) was added 3-[(4-chlorophenyl)thio]-2-methyl-6-(methylsulfonyl)-1H-indole (160 mg) (the product of Example 20 step i). After 30 minutes the reaction was treated with ethyl bromoacetate (78 μl) and stirring continued for 1 hour. Reaction was quenched with ethanol, the solvent was removed in vacuo, the residue redissolved in ethyl acetate, washed with water, dried (MgSO4), and evaporated in vacuo and the residue purified by flash column chromatography eluting with 30% ethyl acetate and iso-hexane mixture. The sub-title compound was obtained as a white solid (180 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166607B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-16c3b861494c4e8c917cee12648ff35a |
| Source note | uspto-grants-2007_01 |