Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066123Generated: October 26, 2026

N,N-Dimethylcyclohexylamine → HCID 178446290, compound

https://huagongshe.com/reaction/1066123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylcyclohexylamineHCID 7415—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant3-Methylbutan-2-amine--hydrogen chloride (1/1)HCID 120793—
Reactant6-chloro-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxideHCID 12487094—
SolventWaterHCID 962—
ProductHCID 178446290HCID 17844629037.4%

Reaction Conditions

Temperature195 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242443B1
Source datasetuspto-grants-2001_06
ORD IDord-f016c12d72c64a0585f8931cb1a8c3fa
Source noteuspto-grants-2001_06