HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325510Generated: October 29, 2026
Triethylamine → 3-Amino-4-[3-(6-piperidinomethyl-2-pyridyloxy)propylamino]-1,2,5-thiadiazole
https://huagongshe.com/reaction/325510
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 4 N 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 | US04440933 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-46ee9491340e49fd9d820170778f89d1 |
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| Source note | uspto-grants-1984_04 |
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