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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096844Generated: October 31, 2026

Sodium Hydroxide → 7-[2-(2-Hydroxyethoxymethyl)thiazol-5-yl]-3,9-diazabicyclo[3.3.1]-non-6-ene-3,6,9-tricarboxylic acid 3,9-di-tert-butyl ester

https://huagongshe.com/reaction/1096844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant7-[2-(2-Hydroxyethoxymethyl)thiazol-5-yl]-3,9-diazabicyclo[3.3.1]-non-6-ene-3,6,9-tricarboxylic acid 3,9-di-tert-butyl ester 6-ethyl esterHCID 86637064—
SolventEthanolHCID 702—
Product7-[2-(2-Hydroxyethoxymethyl)thiazol-5-yl]-3,9-diazabicyclo[3.3.1]-non-6-ene-3,6,9-tricarboxylic acid 3,9-di-tert-butyl esterHCID 8663706856%

Reaction Conditions

Temperature70 °C

Reaction Steps

Aq. 1M NaOH (1.0 mL) was added to a sol. of the compound C5 (50 mg, 0.090 mmol) in EtOH (1.0 mL). The resulting mixture was stirred at 70° C. for 1 h, cooled to rt and the solvent removed in vacuo. The crude mixture was partitioned between Et2O and aq. sat. NH4Cl. The aq. layer was extracted once more with Et2O, then acidified to pH= 4-5, and extracted again with Et2O. The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to yield the title compound (26.4 mg, 56%), which was not further purified. LC-MS: tR=0.82 min, ES+: 526.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138340B2
Source datasetuspto-grants-2012_03
ORD IDord-ce56f1d0d28a4e2b96df3c93fecf2d8c
Source noteuspto-grants-2012_03