HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382476Generated: October 31, 2026
2-Ethylbutyric acid → HCID 69907473, compound
https://huagongshe.com/reaction/382476
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Ethylbutyric acid | HCID 6915 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Ethylbutyryl chloride | HCID 75954 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86757539 | HCID 86757539 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 69907473 | HCID 69907473 | 71.2% |
Reaction Steps
tert-Butyl (R)-N-[2-[7-carbamoyl-1-(3-hydroxy-propyl)-1H-indol-5-yl]-1-methylethyl]-N-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]carbamate (2.00 g) was dissolved in dry pyridine (3 ml), and 2-ethylbutyryl chloride (0.54 g) prepared from 2-ethylbutyric acid and oxalyl chloride was added to the solution. After the mixture was stirred overnight at room temperature, a saturated aqueous sodium bicarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium bicarbonate solution and brine subsequently, and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the residue was purified by column chromatography on silica gel (eluent:hexane/ethyl acetate=2/1) to give white amorphous (R)-3-[5-[2-[N-(tert-butoxycarbonyl)-N-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]-7-carbamoyl-1H-indol-1-yl]propyl 2-ethylbutyrate (1.66 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310086B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-2158b88281ae4f99976e5109611b41c7 |
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| Source note | uspto-grants-2001_10 |
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