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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233952Generated: October 30, 2026

Methanol → HCID 68580211, compound

https://huagongshe.com/reaction/2233952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 53486081HCID 53486081—
ReactantPentafluorophenyl 4-bromo-5-methyl-1H-pyrrole-2-carboxylateHCID 86608241—
SolventSodium MethoxideHCID 10942334—
ProductHCID 68580211HCID 6858021127.1%

Reaction Steps

tert-Butyl [1-(6-chloropyridin-2-yl)piperidin-4-yl]carbamate (Intermediate 66) (300 mg, 0.99 mmol) was dissolved in 0.5 M solution of sodium methoxide in MeOH (9 ml, 4.45 mmol) at room temperature and the mixture was refluxed for 72 h. The solvent was removed in vacuo, extracted with EtOAc then washed with water. The organic phase was concentrated in vacuo and treated with 4 N hydrochloric acid in dioxane (10 ml) for 2 h. The solvent was removed in vacuo and dried to remove excess hydrochloric acid. The solid was dissolved in NMP (3 ml) and pentafluorophenyl 4-bromo-5-methyl-1H-pyrrole-2-carboxylate (Intermediate 17) (80 mg, 0.216 mmol) and TEA (137 μl, 0.9 mmol) were added. The mixture was stirred at room temperature for 2 h and the mixture was purified by semi-preparative HPLC using a gradient of 15-95% CH3CN/H2O (0.1% TFA) to give the title compound (23 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-c1c3bb3a3b4f4f598cd8763f766e0025
Source noteuspto-grants-2010_05