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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990957Generated: October 31, 2026

HCID 16658949, compound → HCID 16659514, compound

https://huagongshe.com/reaction/990957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 16658949HCID 16658949—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 16659514HCID 1665951490%

Reaction Steps

This compound was prepared according to General Method 4 (EXAMPLE 1) from (3R)-3,4-dihydro-3-isopropyl-7-nitro-4-(2,2,2-trifluoroethyl)-2H-1,4-benzoxazine (0.350 g, 1.15 mmol) and 10% Pd/C (0.14 g) in 7 mL EtOAc to afford 0.284 g (90%) of (3R)-7-amino-3,4-dihydro-3-isopropyl-4-(2,2,2-trifluoroethyl)-2H-1,4benzoxazine after purification by flash chromatography (gradient elution, hexanes:EtOAc 9:1 to 3:1). Data for (3R)-7-amino-3,4-dihydro-3-isopropyl-4-(2,2,2-trifluoroethyl)-2H-1,4-benzoxazine: Rf 0.2 (3:1 hexanes:EtOAc); 1H NMR (400 MHz, CDCl3) δ 6.71 (d, 1H, J=8.5), 6.27 (dd, 1H, J=8.5, 2.6), 6.20 (d, 1H, J=2.5), 4.34 (dd, 1H, ABX, J=11.0, 1.5), 3.84 (dd, 1H, ABX, J=11.3, 2.2), 3.71-3.47 (m, 2H), 3.41 (broad s, 2H), 2.62 (d, 1H, J=9.8), 1.81-1.70 (m, 1H), 0.98 (d, 3H, J=6.7), 0.96 (d, 3H, J=6.7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462038B1
Source datasetuspto-grants-2002_10
ORD IDord-dd26c5c8a7b148e9a1504ff0f729b253
Source noteuspto-grants-2002_10