HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634919Generated: October 26, 2026
L-Valine → N-(1,3-Dimethylindole-2-Carbonyl)Valine
https://huagongshe.com/reaction/634919
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Valine | HCID 6287 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1,3-dimethyl-1H-indole-2-carboxylic acid | HCID 12496663 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(1,3-Dimethylindole-2-Carbonyl)Valine | HCID 53637592 | 94.6% |
Reaction Steps
DMAP (367 mg, 3.0 mmol) and EDAC (748 mg, 3.9 mmol) were added as solids to a solution of 1,3-dimethylindole-2-carboxylic acid (568 mg, 3.3 mmol) in DMF (5 mL), and the resultant mixture was stirred for 10 minutes under a nitrogen atmosphere at 0° C. A methylene chloride solution of the methyl ester of valine (553 mg, 3.3 mmol, in 5 mL of methylene chloride) was added to the mixture, and the mixture was first stirred for one hour at 0° C. then for 5 hours at room temperature. The reaction mixture was partitioned between ethyl acetate and 5% KHSO4 solution and the aqueous solution was back-extracted with ethyl acetate. The combined ethyl acetate washes were in turn washed with 5% KHSO4 solution saturated sodium bicarbonate solution (2×) and brine, dried over sodium sulfate, and concentrated to give the title product as a yellow syrup (900 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06184244B2 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-6885d293b51d47c48f15a4473ae7224e |
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| Source note | uspto-grants-2001_02 |
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