HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534603Generated: October 28, 2026
Methyl 5-amino-2,3-dihydrobenzofuran-2-carboxylate → (+)-N4-(3,4-difluorophenyl)-N2-(2,3-dihydro-2-methoxycarbonylbenzofuran-5-yl)-5-fluoro-2,4-pyrimidinediamine
https://huagongshe.com/reaction/534603
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 5-amino-2,3-dihydrobenzofuran-2-carboxylate | HCID 22060823 | — |
| Reactant | 2-chloro-N4-(3,4-difluorophenyl)-5-fluoro-4-pyrimidineamine | HCID 22061049 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (+)-N4-(3,4-difluorophenyl)-N2-(2,3-dihydro-2-methoxycarbonylbenzofuran-5-yl)-5-fluoro-2,4-pyrimidinediamine | HCID 22060930 | — |
Reaction Steps
A mixture of equivalent amount of 2-chloro-N4-(3,4-difluorophenyl)-5-fluoro-4-pyrimidineamine and (±)-5-amino-2,3-dihydro-2-methoxycarbonylbenzofuran in MeOH was shaken in a sealed tube at 80° C. for 48 h, cooled to room temperature and diluted with a mixture of n-hexanes:EtOAc (1:1; v/v). The resulting solid framed was filtered, washed with a mixture of EtOAc:n-hexanes (1:1; v/v), dried and analyzed to give (±)-N4-(3,4-difluorophenyl)-N2-(2,3-dihydro-2-methoxycarbonylbenzofuran-5-yl)-5-fluoro-2,4-pyrimidinediamine. 1H NMR (DMSO-d6): δ 10.21 (bs, 1H), 9.80 (bs, 1H), 8.20 (d, 1H, J=4.8 Hz), 7.94 (bs, 1H), 7.43 (m, 3H0, 7.15 (bd, 1H, J=8.4 Hz), 6.81 (d, 1H, J=8.1 Hz), 5.35 (dd, 1H, J=6.0 and 6.3 Hz), 3.69 (s, 3H), 3.52 (dd, 1H, J=10.5), 3.22 (dd, 1H, J=9.0 and 6.0 Hz); LCMS: purity: 99%; MS (m/e): 417 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853397B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-88cf4eb47e9546abaf0a3363fa31a253 |
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| Source note | uspto-grants-2014_10 |
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