HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57484Generated: October 28, 2026
Diisopropylethylamine → (4R)-3-[2-[[1-[3-(4-Chlorophenyl)-5-isoxazolyl]ethyl]amino]-4-pyrimidinyl]-4-[(1R)-1-(1,1-dimethylethoxy)ethyl]-2-oxazolidinone
https://huagongshe.com/reaction/57484
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(3-(4-Chlorophenyl)isoxazol-5-yl)ethanamine | HCID 83849874 | — |
| Reactant | (R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-one | HCID 90415866 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (4R)-3-[2-[[1-[3-(4-Chlorophenyl)-5-isoxazolyl]ethyl]amino]-4-pyrimidinyl]-4-[(1R)-1-(1,1-dimethylethoxy)ethyl]-2-oxazolidinone | HCID 90415932 | 37.6% |
Reaction Steps
To a solution of 1-(3-(4-chlorophenyl)isoxazol-5-yl)ethanamine (610 mg, 2.74 mmol) and (R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-one (774 mg, 2.74 mmol) in DMSO (5 ml) was added N-ethyl-N-isopropylpropan-2-amine (2 eq, 0.96 mL, 5.48 mmol) and heated in a microwave at 120° C. for 2 hours. Dilute with EtOAc (50 ml), wash with water (50 ml), brine (50 ml), concentrate in vacuo. Flash column chromatography (silica, 40 g) eluting w/0-25% EtOAc/DCM afforded 500 mg of white solid: 1H NMR (400 MHz, CDCl3) b 8.24 (dd, J=5.8, 1.6 Hz, 1H), 7.80-7.65 (m, 2H), 7.58 (dd, J=5.8, 1.6 Hz, 1H), 7.49-7.37 (m, 2H), 6.48-6.35 (m, 1H), 5.66-5.44 (m, 1H), 4.71 (dddd, J=9.8, 8.5, 4.6, 3.0 Hz, 1H), 4.63 (ddd, J=9.4, 3.1, 2.1 Hz, 1H), 4.50-4.26 (m, 2H), 1.71 (s, 1H), 1.25 (s, 5H), 1.15 (s, 5H), 1.03 (dd, J=22.4, 6.4 Hz, 3H), 5.44-5.13 (m, 1H). HRMS(B) tR=3.36 min; m/z 485.1830
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-7d29d564ae4b4bd8a27be73cb98d1ed2 |
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| Source note | uspto-grants-2016_09 |
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