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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189672Generated: October 30, 2026

Dichloromethane → HCID 178482257, compound

https://huagongshe.com/reaction/1189672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
ReactantHCID 178482258HCID 178482258—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178482257HCID 178482257—

Reaction Steps

A mixture of N-(trans-4-trifluoromethyl-cyclohexyl)-2-[N-methyl-N-aminocarbonylmethyl-amino]-4-methylamino-5-nitro-benzoic acid amide (compound IIIa, 45 mg, 0.104 mmol), Burgess reagent (27 mg, 0.11 mmol, +20 mg after 0.5 h, +15 mg after 2.5 h, +20 mg after 16 h), DCM (2 mL) and THF (2 mL) is stirred for 2.5 h at rt, then for 13.5 h at 40° C. and then for 2 h at reflux. The mixture is diluted with sat aq NaHCO3, extracted with EtOAc and the combined organic phases are dried with Na2SO4, filtered and concentrated and directly used in the next step. Yield: 80 mg. HPLC Rt=1.36 min (method A). MS m/z: 414 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674113B2
Source datasetuspto-grants-2014_03
ORD IDord-a8762f9aa2fc4f048fdc6c1917a8854a
Source noteuspto-grants-2014_03