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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292199Generated: October 31, 2026

Water → HCID 69619741, compound

https://huagongshe.com/reaction/1292199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-FluorobenzylamineHCID 67326—
Reactant(R)-2-(Toluene-4-sulfonyloxymethyl)-2,3,8,9-tetrahydro-7H-1,4-dioxino[2,3-e]indol-8-oneHCID 15381104—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 69619741HCID 6961974162%

Reaction Conditions

Temperature85 °C

Reaction Steps

(R)-2-(Toluene-4-sulfonyloxymethyl)-2,3,8,9-tetrahydro-7H-1,4-dioxino[2,3-e]indol-8-one (1.15 g, 3.07 mmole) and 4-fluorobenzylamine (1.56 ml, 13.6 mmole) were combined in 15 ml of dry DMSO and heated to 85° C. for 3.5 hours under a nitrogen atmosphere. After cooling to room temperature, 150 ml of water was added and the mixture was extracted twice with 250 ml portions of 50% ethyl acetate in hexane. The combined organic phases were washed with brine, dried over MgSO4, filtered and concentrated in vacuum to yield an oil, which was column chromatographed on silica gel using 0.75% methanol/CH2Cl2 as eluant. The free base of the title compound (0.62 g, 62%) thus obtained was crystallized from ethanol with the addition of one equivalent of fumaric acid to give 0.69 g of the (S) enantiomer of the title compound as an off-white solid fumarate, m.p. 218°-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756532
Source datasetuspto-grants-1998_05
ORD IDord-5653ab0f85da436f99c7f4d289bfcfc7
Source noteuspto-grants-1998_05