HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426376Generated: November 2, 2026
Trifluoroacetic acid → 5-(Piperidin-4-ylamino)-[1,3,4]thiadiazole-2-carbonitrile
https://huagongshe.com/reaction/1426376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-(5-Cyano-[1,3,4]thiadiazol-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester | HCID 59323571 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Piperidin-4-ylamino)-[1,3,4]thiadiazole-2-carbonitrile | HCID 59323573 | 92% |
Reaction Steps
To a stirred solution of 4-(5-cyano-[1,3,4]thiadiazol-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (D5) (0.973 g, 3.12 mmol) in dichloromethane (55 ml), at 0° C., was added trifluoroacetic acid (3 ml). The reaction mixture was stirred at 0° C. for 1 h. and at room temperature for 18 h. more. After this period, the reaction mixture was extracted with a saturated solution of sodium carbonate. The aqueous layer was extracted with ethyl acetate (2×25 ml). The organic layer was separated, dried (Na2SO4) and the solvent evaporated in vacuo to yield D6 (0.60 g, 92%) as a solid. C8H11N3S requires 209. Found 210 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933101B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-e11f633700ae4335bc69f19ddb3f6d82 |
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| Source note | uspto-grants-2015_01 |
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