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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095682Generated: October 30, 2026

Dimethylformamide → HCID 178429779, compound

https://huagongshe.com/reaction/2095682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant1,4-DioxaneHCID 31275—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantHCID 178429780HCID 178429780—
ProductHCID 178429779HCID 178429779—

Reaction Steps

To a solution of cis-4-(4-iodo-5-methyl-1H-pyrazol-1-yl)cyclohexanol (400.0 mg, 1.306 mmol), triethylamine (0.5463 mL, 3.920 mmol) and DCM (10 mL, 200 mmol) was added methanesulfonyl chloride (0.2022 mL, 2.613 mmol), and the reaction was stirred at rt for 2 h. The material was extracted with DCM and water, which was titrated to pH=5. The organic layer was concentrated in vacuo, redissolved in DMF (5 mL, 60 mmol), and sodium azide (169.9 mg, 2.613 mmol) was added. The mixture was heated to 90° C. for 3 h. The material was extracted with EtOAc, and washed with water (2×). The organic layer was concentrated in vacuo, redissolved in 1,4-dioxane (5 mL, 60 mmol), and PPh3 (514.0 mg, 1.960 mmol) was added. The mixture was heated to 70° C. for 3 h. The solvent was removed in vacuo, and the material was extracted with DCM and water, which was titrated to pH=2. The organic layer was discarded, more DCM was added, and the aqueous layer was titrated to pH=9. The organic layer was concentrated in vacuo to afford the title compound as a light yellow solid. MS (ES+): m/z=306.04 (100) [MH+]. HPLC: tR=0.89 min (polar—3 min, UPLC-ACQUITY).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445510B2
Source datasetuspto-grants-2013_05
ORD IDord-2cdf8865730440639f4f77ffcc5ae837
Source noteuspto-grants-2013_05