Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromo-5,6-diphenyl-furo[2,3-d]pyrimidine | HCID 58603311 | — |
| Reactant | (S)-(tetrahydrofuran-2-yl)-methylamine | HCID 66683780 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Aim-100 | HCID 11501591 | 95% |
Reaction Steps
Compound 69 (60 mg, 0.17 mmol), (S)-tetrahydrofuran-2-yl-methylamine (36 μL, 0.34 mmol), and DIEA 150 μL (0.86 mmol) were mixed in 1-butanol (2 mL) and heated to 120° C. for 1.5 h. The reaction mixture was concentrated, and the residue was purified by flash chromatography to yield a white solid (60 mg). MS: 372.1 (M+1). 1HNMR (DMSO-d6) ppm 8.36 (s, 1H), 7.61-7.34 (m, 10H), 5.11 (t, 1H), 3.89-3.85 (m, 1H), 3.58-3.48 (m, 4H), 1.84-1.64 (m, 3H), 1.40-1.38 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776867B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-b4a3fc13682049a797ecb96830a70510 |
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| Source note | uspto-grants-2010_08 |
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