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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809051Generated: November 1, 2026

Chlorosuccinimide → HCID 59542546, compound

https://huagongshe.com/reaction/1809051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 42644588HCID 42644588—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 59542546HCID 5954254664.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

N-Chlorosuccinimide (0.024 g, 0.18 mmol) was added to a solution of azepan-1-yl-[5-(tetrahydro-pyran-4-yl)-thiophen-3-yl]-methanone (53 mg) in acetic acid (2 mL). The reaction mixture was heated to 100° C. for 3 minutes using microwave irradiation, then diluted with water and purified by HPLC, eluting with 20%-98% acetonitrile in water (0.1% formic acid). The fractions containing the desired product were concentrated under vacuum to give the title compound (38 mg). LCMS m/z 328.17 [M+H]+ RT=10.59 min (Analytical Method 1). 1H NMR (400 MHz, CHCl3-d): δ 6.6 (s, 1H), 4.05 (m, 2H), 3.7 (m, 2H), 3.5 (m, 2H), 3.4 (m, 2H), 2.9 (m, 1H), 1.9-1.5 (m, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362008B2
Source datasetuspto-grants-2013_01
ORD IDord-9ab2f4c687ae47fcbca4715ef06574df
Source noteuspto-grants-2013_01