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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689488Generated: October 30, 2026

Triethylamine → HCID 57989137, compound

https://huagongshe.com/reaction/1689488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Nonanol, 9-bromo-HCID 108700—
Reactant(2-Isopropylthiazol-4-yl)(1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)methanone trifluoroacetateHCID 66964182—
SolventAcetonitrileHCID 6342—
ProductHCID 57989137HCID 57989137—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 9-bromo-1-nonanol (0.316 g) in MeCN (3 mL) was added to solution of (2-isopropylthiazol-4-yl)(1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)methanone trifluoroacetate (example 22, step b) (0.40 g) and triethylamine (0.395 mL) in MeCN (7 mL). The resulting mixture was stirred at 60° C. under argon for 16 h. After cooling to RT the solvent was removed in vacuo. The residue was taken up in DCM, washed with brine (×2), dried over sodium sulphate, filtered and evaporated in vacuo. The orange solid was purified by silica gel chromatography eluting with 0-10% MeOH in DCM to give the subtitled compound as an off-white solid. Yield 0.325 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-c143d005a5ed4d46b037c6d673c706a2
Source noteuspto-grants-2012_04