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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130879Generated: October 27, 2026

Phenethyl bromide → HCID 44434067, compound

https://huagongshe.com/reaction/130879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
Reactant6-(2,3,4,5-tetrahydro-1H-benzo[c]azepin-7-yloxy)nicotinamideHCID 59730216—
SolventDimethylformamideHCID 6228—
ProductHCID 44434067HCID 4443406729%

Reaction Conditions

Temperature75 °C

Reaction Steps

Mix 6-(2,3,4,5-tetrahydro-1H-benzo[c]azepin-7-yloxy)nicotinamide (Part E, 112.9 mg, 0.40 mmol), K2CO3 (110.1 mg, 0.80 mmol), and phenethyl bromide (82 uL 0.60 mmol) in DMF (2.0 mL). Heat at 70-80° C. overnight. Remove DMF azeotropically with xylenes. Purify by flash chromatography, eluting with 75:19:6 EtOAc/CH2Cl2/2.0 M NH3 in MeOH and then with 60:30:10 EtOAc/hexanes/2.0 M NH3 in MeOH. Purify by reverse phase chromatography, eluting with 0-99% 0.1% TFA/acetonitrile and 0.1% TFA/water to give the title compound (44.9 mg, 27% from Step D): MS ES+ 284.0 (M−H)+; HPLC [YMC-Pack Pro C-18 (150×4.6 mm, S-5 microm), 0.1% TFA/acetonitrile in 0.1% TFA/water at 1.0 mL/min, 5-95% over 19 min], tR=9.85 min, 100% purity; Anal. Calcd for C24H25N3O2.0.1H2O.0.1MeOH: C, 73.75; H, 6.57; N, 10.71. Found: C, 73.45; H, 6.62; N, 10.72.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-ca71ab54daf5466c952947ee060e18c6
Source noteuspto-grants-2008_06