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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278310Generated: October 31, 2026

Methanol → HCID 23513777, compound

https://huagongshe.com/reaction/278310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 54304136HCID 54304136—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23513777HCID 23513777—

Reaction Steps

1-(4-Bromo-benzyl)-4-[4-(4-piperidin-1-yl-but-2-ynyloxy)-benzenesulfonyl]-piperdine-4-carboxylic acid was prepared starting from 1-(4-bromo-benzyl)-4-[4-(4-piperidin-1-yl-but-2-ynyloxy)-benzenesulfonyl]-piperidine-4-carboxylic acid ethyl ester (4.64 g, 7.5 mmol) dissolved in THF:methanol (50:150 ml) and 10 N NaOH (20 ml). The resulting reaction mixture was worked up as outlined in Example 1 (Step 7). Yield 3.35 g (76%); off white solid; mp 180° C.; MS: 295.9 (M+2H)2+ 590.9 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358980B1
Source datasetuspto-grants-2002_03
ORD IDord-b47f2b2e0a71486389dd6561ceacd28a
Source noteuspto-grants-2002_03