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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541770Generated: November 3, 2026

Methanesulfonyl chloride → HCID 57961732, compound

https://huagongshe.com/reaction/541770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 66896816HCID 66896816—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 57961732HCID 5796173250.4%

Reaction Steps

To a solution of [6-chloro-2,4,8,22-tetraazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-11-yl]methanol trifluoroacetate (0.731 g, 1.56 mmol) in THF (15 mL) was added methanesulfonyl chloride (151 μL, 1.95 mmol) and N,N-diisopropylethylamine (0.93 mL, 5.32 mmol) at 0° C. The resulting reaction solution was stirred at same temperature for 2 hours. The reaction solution was diluted with DMF (8 mL) and N-tert-butoxycarbonylpiperazine (396 mg, 2.13 mmol) was added, followed by N,N-diisopropylethylamine (0.818 mL, 4.70 mmol). The reaction solution was stirred at 40° C. overnight. The reaction solution was diluted with 1 N HCl solution and ethyl acetate and the aqueous layer was extracted with ethyl acetate once. The aqueous layer was neutralized with 50% NaOH solution to pH 10, and then extracted with EtOAc twice. The combined organic solutions were dried over sodium sulfate, filtered and concentrated. The residue was purified by flash column chromatography to yield the desired product (410 mg, 50%). LCMS calculated for C28H34ClN6O2(M+H)+: m/z=521.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-3fce76274e6c4fc2a50357a09a16c138
Source noteuspto-grants-2014_10