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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401778Generated: November 1, 2026

Tetrahydrofuran → HCID 68304050, compound

https://huagongshe.com/reaction/1401778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetramethylammonium fluorideHCID 67803—
Reactant(6-Bromohexyloxy)-tert-butyldimethylsilaneHCID 4260352—
ReactantHCID 68381095HCID 68381095—
ProductHCID 68304050HCID 68304050—

Reaction Steps

The preparation was carried out as already described starting from 100 mg (0.16 mmol) of 1-[4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)thiazol-2-yl]piperidin-4-ylamine hydrochloride and 90 μl (0.32 mmol) of (6-bromohexyloxy)tert-butyldimethylsilane. The protecting group was cleaved off in THF using 7 equivalent of TMAF. The product was purified by means of preparative HPLC. The product is in the form of the hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907098B2
Source datasetuspto-grants-2014_12
ORD IDord-cc99e5f091ac414eb11891ef4804a16d
Source noteuspto-grants-2014_12