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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053634Generated: October 25, 2026

N-Iodosuccinimide → HCID 178455023, compound

https://huagongshe.com/reaction/1053634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1H-indazoleHCID 58042511—
SolventDimethylformamideHCID 6228—
ProductHCID 178455023HCID 17845502398%

Reaction Steps

To a solution of 5-[(tert-butyldimethylsilyl)oxy]-1H-indazole (13 g, 52.34 mmol, 1.00 equiv) in N,N-dimethylformamide (550 mL) maintained under nitrogen was added NIS (28.6 g, 104.76 mmol, 2.00 equiv) in portions. The reaction mixture was stirred at room temperature overnight and then concentrated under vacuum. The residue was purified on a silica gel column eluted with 0-10% of ethyl acetate in petroleum ether to give 19.2 g (98%) of 5-(tert-butyldimethylsilyloxy)-3-iodo-1H-indazole as an off-white solid. 1H NMR (300 MHz, CDCl3): δ 7.50-7.45 (m, 1H), 7.09 (dd, J=9.0 Hz, 2.1 Hz, 1H), 6.98-6.70 (m, 1H), 1.10 (s, 9H), 0.24 (s, 6H) ppm. LCMS (method A, ESI): RT=1.80 min, m/z=374.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394258B2
Source datasetuspto-grants-2016_07
ORD IDord-eb793d94eabb4d009c81ff497987b181
Source noteuspto-grants-2016_07