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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594169Generated: November 3, 2026

2-tert-Butyl-1,1,3,3-tetramethylguanidine → HCID 72194696, compound

https://huagongshe.com/reaction/594169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-1,1,3,3-tetramethylguanidineHCID 3571581—
Reactant4-((3,5-Dimethylisoxazol-4-yl)methoxy)benzene-1-sulfonyl chlorideHCID 16490702—
ReactantHCID 89876049HCID 89876049—
SolventPyridineHCID 1049—
ProductHCID 72194696HCID 72194696—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of N-(2-methylpropyl)-2-(trifluoromethyl)-4-pyrimidinamine (100 mg, 0.456 mmol) and 4-{[(3,5-dimethyl-4-isoxazolyl)methyl]oxy}benzenesulfonyl chloride (151 mg, 0.502 mmol) in pyridine (1 mL) was added 2-(tert-butyl)-1,1,3,3-tetramethylguanidine (0.092 mL, 0.456 mmol). The reaction vessel was sealed and heated by microwaves to 100° C. for 30 minutes. The solvent was evaporated in vacuo to give the crude product, which was purified by solid phase extraction (SPE) using an aminopropyl (NH2) cartridge then a sulphonic acid (SCX) cartridge (both eluted with methanol). The appropriate fractions were combined and dried under a stream of nitrogen to give the crude product which was further purified by mass directed autoprep (formic acid modifier) to give the title product, 19.8 mg. LCMS (2 min, formic) Rt 1.32 min, m/z (ES+) 485 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242972B2
Source datasetuspto-grants-2016_01
ORD IDord-ca8285e440b049e0b804d18670c43b55
Source noteuspto-grants-2016_01