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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774717Generated: November 2, 2026

Triethylamine → HCID 90221171, compound

https://huagongshe.com/reaction/1774717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 76282920HCID 76282920—
SolventDichloromethaneHCID 6344—
ProductHCID 90221171HCID 90221171—

Reaction Steps

To a solution of 324 (50 mg, 0.1182 mmol) in DCM was added triethylamine (17.9 mg, 0.1773 mmol). Methane sulfonyl chloride 342 (13.5 mg, 0.1182 mmol) was added to the reaction and stirred for 2 h at rt. The reaction mixture was diluted with dichloromethane and washed with water twice. The organic layer was dried over sodium sulphate and concentrated to get the crude, which was purified by flash column using 100-200 mesh silica gel. The compound was eluted at 2% methanol in chloroform as off white coloured solid 3-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-5-(1-(1-(methylsulfonyl)piperidin-4-yl)-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine 343. 1H NMR (400 MHz, DMSO) δ: 11.94 (s, 1H), 8.55 (d, 1H), 8.39 (m, 2H), 8.03 (s, 1H), 7.88 (d, 1H), 7.78 (d, 1H), 7.58 (m, 1H), 7.44 (d, 1H), 4.31 (m, 1H), 3.66 (m, 2H), 2.95 (s, 3H), 2.16 (m, 2H), 2.01 (m, 2H) and MS ES+502.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260426B2
Source datasetuspto-grants-2016_02
ORD IDord-1e06ae8a8be34159bb699e13ad504ace
Source noteuspto-grants-2016_02