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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452884Generated: October 26, 2026

Sodium Bicarbonate → 2-methylsulfonyl-N-[3-(5-methoxy-1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamide

https://huagongshe.com/reaction/1452884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-Boc-5-methoxyindole-2-boronic acidHCID 2794716—
Reactanttert-butyl 3-iodo-5-(N-tert-butoxycarbonyl-2-methylsulfonylbenzenesulfonylamino)indazole-1-carboxylateHCID 22567083—
SolventDimethylformamideHCID 6228—
Product2-methylsulfonyl-N-[3-(5-methoxy-1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamideHCID 13562193919.3%

Reaction Steps

2-Methylsulfonyl-N-[3-(5-methoxy-1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamide can be obtained as described in Example 47 from 1.77 g of tert-butyl 3-iodo-5-(N-tert-butoxycarbonyl-2-methylsulfonylbenzenesulfonylamino)-indazole-1-carboxylate, 1.52 g 1-(tert-butoxycarbonyl)-5-methoxy-indole-2-boronic acid, 70 ml of dimethyl-formamide, 5.65 ml of a saturated aqueous sodium hydrogencarbonate solution and 151 mg of tetrakis(triphenylphosphine)palladium[0]. 250 mg of 2-methylsulfonyl-N-[3-(5-methoxy-1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamide are thus obtained in the form of an amorphous cream solid (LC/MS analysis: Tr 3.52 minutes MH+=497).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473701B2
Source datasetuspto-grants-2009_01
ORD IDord-1865e8e8a8ba4b7aa788204f12d66d2f
Source noteuspto-grants-2009_01