HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514080Generated: November 4, 2026
1,3,4-Thiadiazol-2-amine → HCID 86637650, compound
https://huagongshe.com/reaction/1514080
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3,4-Thiadiazol-2-amine | HCID 19909 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 59138622 | HCID 59138622 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86637650 | HCID 86637650 | 79.3% |
Reaction Steps
A solution of 3-(6-chloro-pyridin-3-yl)-2,2-dimethyl-3-phenyl-propionic acid (Preparation 4, 100 mg, 0.345 mmol), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDC) (132 mg, 0.69 mmol) and 1-hydroxy-7-benzotriazole (HOBt) (93 mg, 0.69 mmol), 1,3,4-thiadiazol-2-amine (103 mg, 1.04 mmol) and diisopropylethyl amine (0.21 ml, 1.21 mmol) in CH3CN (1 mL) was heated at 75° C. for 12 hours. The reaction mixture was filtered, concentrated and purified by silica gel flash chromatography using 50% ethyl acetate in hexanes to give 3-(6-chloro-pyridin-3-yl)-2,2-dimethyl-3-phenyl-N-[1,3,4]thiadiazol-2-yl-propionamide as a white solid. (102 mg, 79.3% yield).). 1H NMR (400 MHz, CDCl3): δ 1.31 (s, 3H), 1.32 (s, 3H), 4.57 (s, 1H), 7.15 (m, 1H), 7.20 (m, 2H), 7.28 (m, 3H), 7.85 (m, 1H), 8.26 (br s, 1H), 8.90 (s, 1H). LC/MS (m/z) 373.19 [(M+H)+]; HPLC Rt: 2.913 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222247B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-d760add0f9af49258188b1656ecc616c |
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| Source note | uspto-grants-2012_07 |
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