HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 6-[(5-Phenylfuro[2,3-d]pyrimidin-4-yl)amino]hexanoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 6-aminohexanoate hydrochloride | HCID 11499324 | — |
| Reactant | 4-Chloro-5-phenylfuro[2,3-d]pyrimidine | HCID 59427833 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-[(5-Phenylfuro[2,3-d]pyrimidin-4-yl)amino]hexanoic acid methyl ester | HCID 58016925 | — |
Reaction Steps
Heat 500 mg (2.19 mmol) 4-chloro-5-phenylfuro[2,3-d]pyrimidine, 1.51 ml (8.67 mmol) DIEA and 1 ml DMF to 160° C. and add 787.6 mg (4.34 mmol) 6-aminohexanoic acid methyl ester hydrochloride. After 4 h at 160° C., cool the reaction mixture, add to ice water and extract three times with ethyl acetate. Combine the organic phases and wash with saturated ammonium chloride solution, dry over magnesium sulphate and concentrate under vacuum. Purify the residue by chromatography on silica gel (solvent: cyclohexane/ethyl acetate 10:1→3:1). 470 mg (63.9% of theor.) of the target compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183246B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-1822757d2f8f48f4a5dea003ec278e57 |
| Source note | uspto-grants-2012_05 |