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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173295Generated: October 30, 2026

HCID 86693013, compound → HCID 86693014, compound

https://huagongshe.com/reaction/2173295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86693013HCID 86693013—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
ProductHCID 86693014HCID 86693014—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 4-[(7-bromo-1-benzofuran-3-yl)methyl]piperazine-1-carboxylate (100 mg, 0.253 mmol), Pd(PPh3)2Cl2 (10 mg, 0.0142 mmol) and TEA (2 mL) in 20 mL of MeOH was heated at 100° C. under CO (3 MPa) overnight. After cooling, the mixture was filtered. The filtrate was then partitioned between EtOAc and water. The combined organics were washed with water (150 mL) and brine (150 mL), dried over Na2SO4 and concentrated to give tert-butyl 4-{[7-(methoxycarbonyl)-1-benzofuran-3-yl]methyl}piperazine-1-carboxylate. 1H-NMR (400 MHz, CDCL3) δ ppm 7.88-7.91 (m, 2H), 7.59 (s, 1H), 7.24 (t, J=7.6 Hz, 1H), 3.94 (s, 3H), 3.59 (s, 2H), 3.30-3.50 (m, 4H), 2.30-2.40 (m, 4H), 1.39 (s, 9H); MS m/z 375 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-3b29281477b248b6ae75620fb1c93df3
Source noteuspto-grants-2015_06