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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896101Generated: November 1, 2026

Potassium Hydroxide → HCID 46912472, compound

https://huagongshe.com/reaction/1896101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 44194039HCID 44194039—
SolventMethanolHCID 887—
ProductHCID 46912472HCID 46912472100.5%

Reaction Steps

(R)-7-[3-Amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine-1-carboxylic acid 3 (100 mg, 0.22 mmol) was dissolved in 5 mL of methanol followed by addition of aqueous potassium hydroxide (0.44 mL, 0.22 mmol). The reaction was stirred for 15 minutes. The reaction mixture was concentrated under reduced pressure to obtain the title compound potassium (R)-7-[3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine-1-carboxylate 6 (108 mg, 100%) as a white solid. HPLC: 92.78%. MS m/z (ESI): 451.2 [M+1]. 1H NMR (400 MHz, CD3OD, ppm): δ 7.31-7.38 (m, 1H), 7.14-7.23 (m, 1H), 5.07-5.27 (m, 2H), 4.26-4.36 (m, 2H), 4.01-4.15 (m, 2H), 3.52-3.60 (m, 1H), 2.80-2.92 (m, 2H), 2.59-2.74 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518946B2
Source datasetuspto-grants-2013_08
ORD IDord-4d86258ce0c8490d831b109e2b6705b2
Source noteuspto-grants-2013_08