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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470262Generated: October 29, 2026

Diisopropylethylamine → HCID 89832315, compound

https://huagongshe.com/reaction/470262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTrimethylsilyl iodideHCID 85247—
Reactant2-Chloro-5-fluoropyrimidineHCID 583466—
ReactantHCID 89832292HCID 89832292—
SolventAcetonitrileHCID 6342—
ProductHCID 89832315HCID 8983231574%

Reaction Steps

To a solution of racemic benzyl 2-benzamido-7a-(3-bromophenyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazine-6-carboxylate (1.6 g, 2.9 mmol) in acetonitrile (60 mL) is added iodotrimethylsilane (1.3 mL, 9.1 mmol). The resultant solution is stirred at ambient temperature for 3 hours and concentrated to dryness. The residue is purified by ion exchange chromatography (first elute with MeOH/CH2Cl2 (¼, 50 mL), followed by 7 N NH3 in MeOH/CH2Cl2 (¼, 50 mL)) to give after evaporation of the solvent 1.7 g of intermediate, N-[7a-(3-bromophenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide. This is then dissolved in 1,4-dioxane (30 mL) and diisopropylethylamine (2.0 mL, 11 mmol) and 5-fluoro-2-chloropyrimidine (850 μL, 8.90 mmol) are added sequentially. The resulting solution is heated at 110° C. for 1 hour before additional diisopropylethylamine (1.0 mL, 5.7 mmol) is added and heating is continued for another 17 hours before it is cooled to room temperature and concentrated to dryness. The residue is purified by silica gel flash chromatography, eluting with gradient of ethyl acetate/dichloromethane (0% to 30%) to give the title compound (1.1 g, 73%). ES/MS (m/z): (79Br/81Br) 512/514 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629270B2
Source datasetuspto-grants-2014_01
ORD IDord-17ea72e1f2ac4cf0af7456c968ee4178
Source noteuspto-grants-2014_01