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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239456Generated: October 29, 2026

2,6-Difluorobenzenesulfonyl chloride → HCID 57989671, compound

https://huagongshe.com/reaction/239456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluorobenzenesulfonyl chlorideHCID 2734271—
ReactantHCID 57989700HCID 57989700—
ProductHCID 57989671HCID 57989671—

Reaction Steps

Following a procedure analogous to the procedure described in Intermediate 14 using 3-[5-(2-chloro-4-pyrimidinyl)-2-(4-morpholinyl)-1,3-thiazol-4-yl]-2,4-difluoroaniline (900 mg, 2.196 mmol) and 2,6-difluorobenzenesulfonyl chloride (0.357 mL, 2.64 mmol) the title compound of Step A was obtained as a light yellow solid (857 mg, 66% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.89 (s, 1H), 8.40 (d, J=5.5 Hz, 1H), 7.64-7.72 (m, 1H), 7.49-7.56 (m, 1H), 7.21-7.32 (m, 3H), 6.55 (d, J=5.3 Hz, 1H), 3.70-3.74 (m, 4H), 3.52-3.55 (m, 4H). MS (ESI): 585 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642759B2
Source datasetuspto-grants-2014_02
ORD IDord-0d792fd4b1a9429f925ac76275afc9ad
Source noteuspto-grants-2014_02