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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713404Generated: October 29, 2026

Water → HCID 59463859, compound

https://huagongshe.com/reaction/1713404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 59463837HCID 59463837—
SolventDichloromethaneHCID 6344—
ProductHCID 59463859HCID 5946385991%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) suspension of 1-(3,5-Difluoro-benzyl)-3-(2-nitro-phenylsulfanyl)-1H-indole-6-carboxylic acid amide (15 mg, 0.034 mmol) and Et3N (10 μL, 0.072 mmol) in CH2Cl2 (1.5 mL) was added Tf2O (13 μL, 0.077 mmol). The mixture was stirred at 0° C. for 2 h and then at room temperature for 20 h. Water (25 mL) was added and the mixture was extracted with CH2Cl2 (2×25 mL). The combined organic phases were dried (Na2SO4) and concentrated to give the title compound as a yellow solid (13 mg, yield: 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795280B2
Source datasetuspto-grants-2010_09
ORD IDord-6c070b4d75ff4db8b8d7b3b6fefc5f92
Source noteuspto-grants-2010_09