HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 10107810, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | Ethyl 3-amino-1H-indole-2-carboxylate | HCID 732887 | — |
| Solvent | Dichloromethane ethylacetate | HCID 21226138 | — |
| Product | HCID 10107810 | HCID 10107810 | 17.7% |
Reaction Steps
Heat a mixture of ethyl 3-aminoindole-2-carboxylate (204 mg, 1.0 mmol) and 2-chloropyrimidine (1.2 g, 10.5 mmol) at 100° C. for 16 h. Cool the reaction and add aqueous ammonium chloride and ethyl acetate. Filter off excess 2-chloropyrimidine, separate the organic layer, dry with MgSO4, filter and concentrate to afford a crude mixture. Flash chromatograph the mixture on silica gel eluting with 25% ethyl acetate/dichloromethane to afford 50 mg of the title compound: MS 283 (M+H), TLC (silica gel, 25% ethyl acetate/dichloromethane) Rf=0.44.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169925B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-a547485a581749eb9f64f5b4bf0afb1f |
| Source note | uspto-grants-2007_01 |