Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-amino-2,3-dihydrobenzofuran-2-carboxylateHCID 22060823—
Reactant2-chloro-N4-(3,4-difluorophenyl)-5-fluoro-4-pyrimidineamineHCID 22061049—
SolventMethanolHCID 887—
Product(+)-N4-(3,4-difluorophenyl)-N2-(2,3-dihydro-2-methoxycarbonylbenzofuran-5-yl)-5-fluoro-2,4-pyrimidinediamineHCID 22060930—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853397B2
Source datasetuspto-grants-2014_10
ORD IDord-88cf4eb47e9546abaf0a3363fa31a253
Source noteuspto-grants-2014_10