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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422070Generated: October 23, 2026

Water → 5-Iodo-1-(2-(pyrrolidin-1-yl)ethyl)-1H-indazole

https://huagongshe.com/en/reaction/422070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant1-(2-Chloroethyl)pyrrolidine hydrochlorideHCID 81668—
Reactant5-Iodo-1H-indazoleHCID 21894739—
SolventDimethyl SulfoxideHCID 679—
Product5-Iodo-1-(2-(pyrrolidin-1-yl)ethyl)-1H-indazoleHCID 5801554452.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

1-(2-Chloroethyl)pyrrolidine hydrochloride (9.88 g, 58.1 mmol) was added to a suspension of 5-iodo-1H-indazole (8.86 g, 36.3 mmol) and Cs2CO3 (50.8 g, 456 mmol) in anhydrous DMSO (100 mL) and the resulting suspension was stirred at 25° C. for 14 h. H2O (100 mL) was added and the aqueous solution was extracted with EtOAc (3×200 mL). The combined organic extracts were washed with brine (2×200 mL), dried over MgSO4 and concentrated under reduced pressure. Flash chromatography on silica gel (9:1 Et2O/Et3N) afforded 6.473 g (52%) of the title compound as a yellow solid: 1H NMR (300 MHz, CDCl3) δ 8.08 (br d, J=13 Hz, 1H), 7.91 (d, J=0.9 Hz, 1H), 7.60 (dd, J=87, 1.3 Hz, 1H), 7.25 (d, J=8.7 Hz, 1H), 4.50 (t, J=7.4 Hz, 2H), 2.98 (t, J=7.4 Hz, 2H), 2.59-2.50 (m, 4H), 1.82-1.70 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101632B2
Source datasetuspto-grants-2012_01
ORD IDord-a9ea4691af474979b04bf4a15292f509
Source noteuspto-grants-2012_01