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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470802Generated: October 30, 2026

Iodine → HCID 67006036, compound

https://huagongshe.com/reaction/470802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDichloromethaneHCID 6344—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 67006002HCID 67006002—
ProductHCID 67006036HCID 67006036—

Reaction Steps

Triphenylphosphine (1.0 g, 3.85 mmol) was dissolved in 25 mL of DCM followed by addition of I2 (977 mg, 3.85 mmol) and TEA (779 mg, 7.70 mmol) at 0° C. 3-(tert-butyldimethylsilyloxy)-N′-((2R,3S)-3-(tert-butyldimethylsilyloxy)-2-(3-chloro-4-cyano-2-methylphenylamino)butanoyl)-4-fluorobenzohydrazide (1.25 g, 1.93 mmol) in 35 mL DOA was added to the pre-cooled solution mixture of PPh3/I2/TEA system and stir. The temperature was allowed to rise to room temperature and stirred for additional 10 min. The reaction was quenched with 100 mL saturated sodium thiosulfate and extracted with EtOAc. The crude mixture was chromatographed to give the product (1.10 g). 1H NMR (400 MHz, DMSO-d6, δ in ppm): 7.71 (m, 1H), 7.70 (d, J=9 Hz, 1H), 7.65 (m, 1H), 7.03 (d, J=9 Hz, 1H), 6.53 (d, J=9 Hz, 1H), 5.15 (d, J=9 Hz, 1H), 4.80 (m, 1H), 2.44 (s, 3H), 1.51 (d, J=6 Hz, 3H), 1.13 (s, 9H), 0.83 (s, 9H), 0.36 (s, 6H), 0.19 (s, 3H), 0.00 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629167B2
Source datasetuspto-grants-2014_01
ORD IDord-fff0cfe3920a4a27b83b515b1ddccd3f
Source noteuspto-grants-2014_01