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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753187Generated: November 2, 2026

Hydrochloric Acid → HCID 67367203, compound

https://huagongshe.com/reaction/1753187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67368547HCID 67368547—
SolventWaterHCID 962—
ProductHCID 67367203HCID 67367203—

Reaction Steps

A solution of 1-{4-bromo-1-[2-(5-methylpyrazin-2-yl)-2-oxoethyl]-1H-pyrrol-2-yl}-2,2,2-trichloroethanone (157 mg, 0.37 mmol) in methanol (7 mL) was treated with sodium hydroxide (15 mg, 0.37 mmol) in water (0.4 mL) at 0° C. and the mixture stirred at room temperature. After one hour the reaction was complete (monitored by LCMS). The mixture was acidified with a aqueous solution of HCl (1 M) and then extracted with CH2Cl2 (3 times). The organic were then dried (Na2SO4), filtrated and concentrated in vacuo to give methyl 4-bromo-1-[2-(5-methylpyrazin-2-yl)-2-oxoethyl]-1H-pyrrole-2-carboxylate (140 mg). The crude was used in the next step without purification. 1H-NMR (400 MHz, CDCl3): δ 2.69 (s, 3H), 3.71 (s, 3H), 5.86 (s, 2H), 6.83 (d, 1H, 1.9 Hz), 7.01 (d, 1H, J 1.9 Hz), 8.53 (s, 1H), 9.13 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163029B2
Source datasetuspto-grants-2015_10
ORD IDord-77efb34ff12346c3ac5571524dfd3809
Source noteuspto-grants-2015_10