HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280417Generated: October 28, 2026
Triethylamine → 3-Amino-4-[3-(6-piperidinomethyl-2-pyridyloxy)propylamino]-1,2,5-thiadiazole
https://huagongshe.com/reaction/280417
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2'-Thiobis(1H-isoindole-1,3(2H)-dione) | HCID 82196 | — |
| Reactant | HCID 178478601 | HCID 178478601 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Amino-4-[3-(6-piperidinomethyl-2-pyridyloxy)propylamino]-1,2,5-thiadiazole | HCID 13313698 | — |
Reaction Steps
A mixture of the crude product prepared in Step B in 80 ml of CH2Cl2 and containing 7.69 ml of triethylamine was treated with N,N'-thiobisphthalimide (DMF solvate) (7.35 g; 18.5 mmoles). After stirring at ambient temperature for one hour, the mixture was washed with 50 ml of 4N NaOH, water, saturated aqueous NaCl solution, dried (Na2SO4), filtered and evaporated under reduced pressure to give the crude product. The product was purified by flash chromatography on 100 g of silica gel (230-400 mesh) using ethyl acetate-methanol (95:5) as the eluent to give 3.63 g of the title compound as a viscous oil. Treatment of the product with one equivalent of cyclohexyl sulfamic acid in acetone gave the cyclohexyl sulfamate salt of the title compound, mp 125.5°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04588826 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-b518097b62104a219533e83bb05f7b98 |
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| Source note | uspto-grants-1986_05 |
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