HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066123Generated: October 26, 2026
N,N-Dimethylcyclohexylamine → HCID 178446290, compound
https://huagongshe.com/reaction/1066123
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylcyclohexylamine | HCID 7415 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 3-Methylbutan-2-amine--hydrogen chloride (1/1) | HCID 120793 | — |
| Reactant | 6-chloro-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide | HCID 12487094 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178446290 | HCID 178446290 | 37.4% |
Reaction Steps
Phosphorus pentoxide (7.55 g, 53.2 mmol), N,N-dimethylcyclohexylamine (17 ml, 113 mmol) and 1,2-dimethylpropylamine hydrochloride (12.4 g, 100.4 mmol) were carefully mixed and heated with mechanical stirring on an oil bath at 190-200° C. for about 15 min. To the homogeneous mass was added 6-chloro-3,4-dihydro-3-oxo-1,2,4-benzothiadiazine 1,1-dioxide (5.84 g, 25.1 mmol) and the mixture was stirred at 235° C. for 2 h. After cooling to about 100° C., water (200 ml) was added and the dark mixture was hydrolysed by stirring over night at room temperature. The precipitate was isolated by filtration and recrystallised from ethanol with decolorising charcoal to give 2,83 g (37%) of the pure title compound; m.p. (DSC) 264.7° C.; 1H-NMR (DMSO-d6): δ 0.90 (dd, 6H, CH(CH3)2), 1.09 (d, 3H, NCHCH3), 1.76 (m, 1H, CH(CH3)2), 3.70 (m, 1H, NHCH), 7.15 (br., 1H, NH), 7.28 (m, 2H, ArH), 7.68 (d, 1H, ArH), 10.3 (br.s, 1H, NH); (C12H16N3Cl1O2S1) calc. C, 47.76; H, 5.34; N 13.92; found C, 47.66; H, 5.47; N, 13.91.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06242443B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-f016c12d72c64a0585f8931cb1a8c3fa |
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| Source note | uspto-grants-2001_06 |
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