HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907540Generated: October 26, 2026
3,4-Dichloro-1,2,5-thiadiazole → 4-(4-Chloro-[1,2,5]thiadiazol-3-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/907540
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-Dichloro-1,2,5-thiadiazole | HCID 79804 | — |
| Reactant | Tert-butyl 1,4-diazepane-1-carboxylate | HCID 2756058 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Chloro-[1,2,5]thiadiazol-3-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester | HCID 59013953 | 79.1% |
Reaction Steps
A mixture of t-butyl 1-homopiperazine carboxylate (45 mmol, 9 g) and DMF (50 ml) was heated to 100° C. 3,4-dichloro-1,2,5-thiadiazole (23 mmol, 2.2 ml) was added to the mixture and stirred at 100° C. for 2 days. The mixture was quenched with ice/water and extracted with ethyl acetate (3×). The combined organic layer was washed with water (2×) and brine, dried over sodium sulfate, filtered and concentrated. The crude was purified on silica column using 20% ethyl acetate/hexanes to give 5.8 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013156B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-d803f609959c4183888beaf29cc87194 |
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| Source note | uspto-grants-2011_09 |
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