HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176435Generated: October 30, 2026
Phosphorus oxychloride → HCID 66668846, compound
https://huagongshe.com/reaction/2176435
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl malonyl chloride | HCID 123460 | — |
| Reactant | 5-(3-Nitrophenyl)-1,3,4-thiadiazol-2-amine | HCID 256343 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66668846 | HCID 66668846 | 32.7% |
Reaction Steps
In a particular instance, the compound of this example is prepared as described or similarly described as follows: To 5-(3-nitrophenyl)-1,3,4-thiadiazol-2-amine (2) (3.0 g, 13.50 mmol) in MeCN (120 ml) is added methyl 3-chloro-3-oxopropanoate (1.735 mL, 16.20 mmol). The mixture is stirred at room temperature for 2 hours. After consumption of the starting material, POCl3 (60 mL, 644 mmol) is added along with DIPEA (2.358 mL, 13.50 mmol) in MeCN (10 mL). The mixture is heated in the microwave at 150° C. for 25 min, cooled, and concentrated in vacuo. The resulting slurry is taken up in chloroform, poured over ice and washed with saturated NaHCO3, water and brine, dried over MgSO4, and concentrated in vacuo to give a dark red oil which is purified via column chromatography on a 100 g snap column with 0-10% EtOAc/DCM gradient elution to give 7-chloro-2-(3-nitrophenyl)-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one (1.36 g, 4.41 mmol, 32.6% yield) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09066948B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-6b17d660eb8a46fc9d1072c8dac34e33 |
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| Source note | uspto-grants-2015_06 |
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