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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867417Generated: October 27, 2026

Sodium Chloride → HCID 68432201, compound

https://huagongshe.com/reaction/1867417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTriethylamineHCID 8471—
Reactant4-(Methylamino)tetrahydro-2H-pyranHCID 6991950—
ReactantN-methyloxan-4-amine hydrochlorideHCID 22736998—
ReactantHCID 68433016HCID 68433016—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
SolventDimethylacetamideHCID 31374—
ProductHCID 68432201HCID 684322014%

Reaction Steps

A solution of 0.100 g (0.20 mmol) of 1-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-4-(4-iodo-butyl)-[1,4]diazepan-5-one (example 9B) in 3.1 ml of DMA was treated with free methyl-(tetrahydro-pyran-4-yl)-amine in 1 ml of toluene [0.035 g (0.22 mmol) methyl-(tetrahydro-pyran-4-yl)-amine hydrochloride were dissolved in 0.8 ml of 0.5 N NaOH was extracted with toluene (2 ml). The organic phase was dried over Na2SO4] and stirred for 22 h at RT, 0.06 ml (0.40 mmol) of Et3N was added and stirring was continued for 18 h at 50° C. Again methyl-(tetrahydro-pyran-4-yl)-amine in 1 ml of CH2Cl2 [0.035 g (0.22 mmol) methyl-(tetrahydro-pyran-4-yl)-amine hydrochloridewere dissolved in 0.5 ml aqueous 10% NaCl solution/0.4 ml of 1 N NaOH was extracted with CH2Cl2 (1 ml). The organic phase was dried over Na2SO4] was added and heated for 9 h at 50° C. The reaction was extracted with aqueous saturated NaHCO3/Et2O (3×). The organic phases were washed with aqueous 10% NaCl, dried (Na2SO4), concentrated and evaporated. Purification by catridges, Si-Amine, 70 ml, 20 g (n-heptane/EtOAc 1:4 to 1:9) gave 0.004 g (4%) of the title compound as a light yellow semisolid. MS: 482.3 (MH+, 2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632829B2
Source datasetuspto-grants-2009_12
ORD IDord-ee4535f1353644dd899932844f6a0895
Source noteuspto-grants-2009_12