HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485367Generated: October 30, 2026
Water → Phenyl (3-methoxy-1,2,4-thiadiazol-5-yl)carbamate
https://huagongshe.com/reaction/1485367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 5-Amino-3-methoxy-1,2,4-thiadiazole | HCID 314179 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenyl (3-methoxy-1,2,4-thiadiazol-5-yl)carbamate | HCID 89664142 | — |
Reaction Steps
3-Methoxy-1,2,4-thiadiazol-5-amine a (500 mg, 3.82 mmol) and phenyl carbonochloridate b (600 mg, 3.82 mmol) were dissolved in 20 mL of dichloromethane, followed by addition of triethylamine (0.8 mL, 5.73 mmol). After reacting for 16 hours, 30 mL of H2O were added into the reaction mixture to dilute the solution. The aqueous phase and organic phase were separated, the aqueous phase was extracted with dichloromethane (20 mL×2), and the organic phases were combined, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography with elution system A to obtain the title product phenyl(3-methoxy-1,2,4-thiadiazol-5-yl)carbamate c (200 mg, yield 20.8%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422300B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-b4051da75b034c87b5f5f3736894c63d |
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| Source note | uspto-grants-2016_08 |
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