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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497300Generated: October 30, 2026

1,1'-Thiocarbonyldiimidazole → HCID 117856679, compound

https://huagongshe.com/reaction/1497300

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
ReactantHCID 89315948HCID 89315948—
SolventDimethylformamideHCID 6228—
ProductHCID 117856679HCID 11785667983.3%

Reaction Steps

To a solution of (1S,2S,3S,4R,5R)-2-amino-3-fluoro-5-(hydroxymethyl)cyclohexane-1,4-diol (480 mg, 2.68 mmol) in DMF (5 mL) at room temperature was added thiocarbonyldiimidazole (549 mg, 3.08 mmol). The mixture was stirred at room temperature for 1.5 h. Solvent was evaporated and the residue was purified by silica gel column chromatography, eluted with 10%-35 MeOH in DCM to give the product (3aS,4S,5R,6R,7aS)-4-fluoro-5-hydroxy-6-(hydroxymethyl)hexahydrobenzo[d]oxazole-2(3H)-thione (494 mg, 83%) as a pale yellow solid. 1H NMR (500 MHz, MeOD) δ 4.74-4.77 (m, 1H), 4.56 (ddd, J=52.8 Hz, 3.8 Hz, 1.7 Hz, 1H), 3.98 (ddd, J=23.3 Hz, 7.0 Hz, 3.9 Hz, 1H), 3.59-3.64 (m, 2H), 3.45 (ddd, J=29.6 Hz, 10.6 Hz, 1.5 Hz, 1H), 2.22-2.27 (m, 1H), 1.95-2.02 (m, 1H), 1.69-1.75 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199949B2
Source datasetuspto-grants-2015_12
ORD IDord-e24b090254544151b1ca404089f2e065
Source noteuspto-grants-2015_12