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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877931Generated: October 31, 2026

Sodium Carbonate → HCID 58827084, compound

https://huagongshe.com/reaction/1877931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPotassium HydroxideHCID 14797—
ReactantTrimethylboroxineHCID 574072—
Reactant3-bromo-4-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)benzonitrileHCID 58827057—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 58827084HCID 58827084—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 3-bromo-4-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)benzonitrile (0.100 g, 0.347 mmol) given in Example 3 (table 2) and trimethylboroxine (0.145 g, 1.04 mmol) in DME (3 mL), aqueous solutions of Na2CO3 (0.69 mL, 2 M) and KOH (0.17 mL, 2 M) are added. After degassing with nitrogen, Pd(PPh3)4 (0.040 g, 0.035 mmol) is added. The mixture is heated in a microwave reactor at 130° C. 1.5 h. At that point LCMS showed consumption of the starting material. The solution is diluted with ethyl acetate and saturated sodium bicarbonate. The resulting aqueous layer is extracted further with ethyl acetate (3×). The combined organic layers are washed with brine and dried over anhydrous sodium sulfate. After concentration the crude product is filtered through 0.45 μm filter and then purified by preparative HPLC (0% for 5 minutes and 0-34% acetonitrile with 0.1% TFA in 17 minutes). MS (ESI) m/z 224.0 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 2.33-2.42 (m, 1 H), 2.43 (s, 3 H), 2.84-2:95 (m, 2 H), 3.07-3.18 (m, 1 H), 5.54 (dd, J=8.1, 4.8 Hz, 1 H), 6.65 (d, J=8.1 Hz, 1 H), 6.83 (s, 1 H), 7.32 (s, 1 H), 7.41 (d, J=8.1 Hz, 1 H), 7.50 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-d33e09ee3a1a4b29926104a378a2a17d
Source noteuspto-grants-2012_11