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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405109Generated: November 4, 2026

Water → HCID 53353199, compound

https://huagongshe.com/reaction/2405109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 67354559HCID 67354559—
SolventDimethylformamideHCID 6228—
ProductHCID 53353199HCID 5335319927%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a 125 ml round bottom flask, 4-(2-hydroxypropan-2-yl)-N-(1-methyl-1H-pyrrolo[3,2-c]pyridin-6-yl)benzamide (2.8 g, 9.05 mmol) was dissolved in DMF (25 ml). To this was added N-chlorosuccinimide (1.5 g, 11 mmol) and the mixture was stirred at 50° C. for 3 hours. The mixture was then poured into 50 ml water and then extracted with ethyl acetate (3×100 ml). Combined organic layers were dried over sodium sulfate and concentrated. The residue was purified by preparatory HPLC (RFA-mode: eluting with 25-55% ACN in water). Fractions containing the desired mono chlorinated product were combined and concentrated. To the residue was added saturated NaHCO3 and the aqueous mixture was extracted with ethyl acetate (2×100 ml). Combined organic layers were dried over sodium sulfate, filtered and concentrated to obtain the title compound (840 mg, 27% yield) as a tan solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.25-1.26 (m, 1H) 1.46 (s, 139H) 3.66-3.86 (m, 3H) 5.17 (s, 1H) 7.40-7.69 (m, 3H) 8.01 (d, J=8.59 Hz, 2H) 8.34 (s, 1H) 8.59 (s, 1H) 10.68 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802695B2
Source datasetuspto-grants-2014_08
ORD IDord-6486539774224920832ea2b42f92e452
Source noteuspto-grants-2014_08