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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452855Generated: October 26, 2026

Trimethylsilyl iodide → HCID 178434307, compound

https://huagongshe.com/reaction/1452855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantN-(N-tert-butoxycarbonyl-3-methyl-1H-indazol-5-yl)-3,4-dichlorobenzenesulfonamideHCID 22567170—
SolventChloroformHCID 6212—
ProductHCID 178434307HCID 17843430780.1%

Reaction Steps

3,4-Dichloro-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 6 from 0.8 g of N-(N-tert-butoxycarbonyl-3-methyl-1H-indazol-5-yl)-3,4-dichlorobenzenesulfonamide, 7.1 ml of chloroform and 0.25 ml of iodotrimethylsilane. 0.5 g of 3,4-dichloro-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide is thus obtained in the form of a white solid melting at 184° C. (analysis: C14H11Cl2N3O2S.0.04CH2Cl2 % calculated, C, 47.21; H, 3.11; Cl, 19.90; N, 11.80; O, 8.98; S, 9.00. % found C, 47.65; H, 2.56; Cl, 19.97; N, 11.89; S, 8.92).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473701B2
Source datasetuspto-grants-2009_01
ORD IDord-d3ad73f9dc7c45c69ca5f3d449885179
Source noteuspto-grants-2009_01