HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853714Generated: October 31, 2026
1,3,4-Thiadiazol-2-amine → HCID 10410705, compound
https://huagongshe.com/reaction/853714
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3,4-Thiadiazol-2-amine | HCID 19909 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 58928692 | HCID 58928692 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10410705 | HCID 10410705 | 40% |
Reaction Steps
9-Benzhydryloxy-7-(4-fluoro-benzyl)-8-oxo-7,8-dihydro-6H-pyrrolo[3,4-g]quinoline-5-carboxylic acid 213 (0.02 g, 0.0386 mmol) was dissolved in 0.3 mL of dimethylformamide. To this was added 2-amino-1,3,4-thiadiazole (0.0078 mL, 0.0772 mmol), diisopropylethylamine (0.027 mL, 0.1544 mmol), O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.03 g, 0.0772 mmol) and stirred at room temperature. After 15 hours, starting material was consumed. Purified by reverse phase HPLC (0.1% TFA, H2O/ACN) to give 7-(4-fluoro-benzyl)-9-hydroxy-8-oxo-7,8-dihydro-6H-pyrrolo[3,4-g]quinoline-5-carboxylic acid [1,3,4]thiadiazol-2-ylamide 320 (0.0066 g, 0.015 mmol, 40%.) 1H NMR (CDCl3) δ 9.02 (dd, 1H), 8.81 (s, 1H), 8.65 (d, 1H), 7.65 (dd, 1H), 7.38 (dd, 2H), 7.05 (dd, 2H), 4.74 (s, 2H), 4.64 (s, 2H.) MS: 436 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253180B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-80faaad9426a4da79b385b2ec0f2cc39 |
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| Source note | uspto-grants-2007_08 |
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