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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400804Generated: November 1, 2026

Cyclopropylamine → HCID 67442248, compound

https://huagongshe.com/reaction/1400804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantHCID 67442310HCID 67442310—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67442248HCID 67442248—

Reaction Conditions

Temperature-25 °C

Reaction Steps

To a stirred solution of aniline 23 (500 mg, 0.92 mmol) and DIPEA (0.8 mL, 4.61 mmol) in THF (18 mL) at −25° C. under nitrogen was added dropwise a solution of triphosgene (273 mg, 0.920 mmol) in THF (2 mL). The reaction mixture was stirred at −25° C. and cyclopropylamine (0.32 mL, 4.61 mmol) was slowly added. The reaction mixture was allowed to warm to RT over 1.5 h and stirred at RT overnight. The reaction mixture was then partitioned between AcOEt and water. The organic layer was successively washed with a saturated aqueous solution of ammonium chloride, 1N NaOH and brine, dried over anhydrous magnesium sulfate, filtered and concentrated to afford the title compound 24 as an off-white solid. The crude material was used in the next step without any further purification. MS (m/z): 626.6 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906852B2
Source datasetuspto-grants-2014_12
ORD IDord-c000547d4f084262b51bf5af04b2f6f8
Source noteuspto-grants-2014_12