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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349708Generated: October 28, 2026

Guanidine → HCID 22480344, compound

https://huagongshe.com/reaction/1349708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidineHCID 3520—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22480020HCID 22480020—
SolventMethanolHCID 887—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 22480344HCID 224803443%

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of 1-[3-(4-fluorophenyl)-1H-indazol-5-yl]ethan-1-one (73 mg, 0.29 mmol) in dimethoxy DMF acetal (25 mL) was heated to 90° C. overnight. The solution was then concentrated to an oil under vacuo when methanol (10 mL), guanidine (55 mg, 0.57 mmol), and NaOMe (290 μL of a 2 N solution, 0.58 mmol) was added. The reaction was then heated in a sealed tube to 120° C. overnight. The reaction was then acidified with trifluoroacetic acid then subjected to preparative HPLC (CH3CN/water 0.1% TFA) to recover the final compound (3 mg, 3% yield). 1H NMR (DMSO-d6) δ 13.5 (br s, 1H), 8.78 (s, 1H), 8.35 (d, 1H), 8.19 (d, 1H), 8.06 (dd, 2H), 7.72 (d, 1H), 7.53 (d, 1H), 7.38 (t, 2H); ES-MS (m/z) 306 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211594B2
Source datasetuspto-grants-2007_05
ORD IDord-6579af43b34648a39f7785f46252ed22
Source noteuspto-grants-2007_05