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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-tert-Butyl-1,1,3,3-tetramethylguanidine | HCID 3571581 | — |
| Reactant | 4-((3,5-Dimethylisoxazol-4-yl)methoxy)benzene-1-sulfonyl chloride | HCID 16490702 | — |
| Reactant | HCID 89876049 | HCID 89876049 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 72194696 | HCID 72194696 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09242972B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-ca8285e440b049e0b804d18670c43b55 |
|---|
| Source note | uspto-grants-2016_01 |
|---|