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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782147Generated: October 31, 2026

2-(2-Bromoethyl)-1,3-dioxolane → HCID 68828677, compound

https://huagongshe.com/reaction/1782147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Bromoethyl)-1,3-dioxolaneHCID 87776—
ReactantHCID 54757413HCID 54757413—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 68828677HCID 6882867795.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 6-(1-amino-2-methyl-propyl)-5-benzyl-3-methyl-5H-isothiazolo[5,4-d]pyrimidin-4-one (method 30) (1.6 g, 4.88 mmol) in anhydrous DMF (20 mL), 2-(2-bromo-ethyl)-[1,3]dioxolane (0.88 g, 4.88 mmol) was added and the resulting solution was heated at 70° C. for 2 h. The reaction mixture was cooled, diluted with water and extracted with EtOAc (3×60 mL). The combined organic extracts were dried (Na2SO4) and concentrated to provide the crude product (2 g), which was used as such in the next reaction. m/z 429 (MH+); 1H-NMR (300 MHz) δ 0.88 (d, 3H), 0.96 (d, 3H), 1.54-1.62 (m, 2H), 1.86-2.05 (m, 2H), 2.18 (bs, 1H), 2.38-2.46 (m, 1H), 2.84 (s, 3H), 3.57 (d, 1H), 3.74-3.94 (m, 4H), 4.78 (t, 1H), 4.99 (d, 1H), 5.85 (d, 1H), 7.15-7.38 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498333B2
Source datasetuspto-grants-2009_03
ORD IDord-8f987da265dd4e879f128a121cab73a6
Source noteuspto-grants-2009_03