HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467679Generated: October 29, 2026
Methylamine → Carbamic acid, N-[4-[(methylamino)carbonyl]-1,2,3-thiadiazol-5-yl]-, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/467679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 70116272 | HCID 70116272 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Carbamic acid, N-[4-[(methylamino)carbonyl]-1,2,3-thiadiazol-5-yl]-, 1,1-dimethylethyl ester | HCID 70115888 | — |
Reaction Steps
A solution of 5-tert-butoxycarbonylamino-[1,2,3]thiadiazole-4-carboxylic acid (0.66 g, 2.7 mmol) in DMF (10 ml) was treated with TBTU (1.16 g, 3.5 mmol), N,N-diisopropyl ethyl amine (2.29 ml, 13.5 mmol) and methylamine (1.75 ml, 2M THF solution) and stirred at ambient temperature for 5 h. The reaction mixture was partitioned between potassium hydrogen sulfate (30 ml, 10% aqueous solution) and ethyl acetate (60 ml) and extracted. The organic layer was washed with water and brine, and the aqueous phases were back-extracted with ethyl acetate. The combined organic phases were dried and the solvent was evaporated. The residue was suspended in dichloromethane, sucked off, and the filtrate was evaporated. The product was obtained after purification of the crude material by silica gel chromatography using a heptane/ethyl acetate gradient as colorless solid (0.23 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08623866B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-512f283ee4b24a93a4703055f7dcf886 |
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| Source note | uspto-grants-2014_01 |
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