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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593069Generated: October 30, 2026

Sodium borohydride → HCID 58998410, compound

https://huagongshe.com/reaction/1593069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58998412HCID 58998412—
SolventEthanolHCID 702—
ProductHCID 58998410HCID 58998410—

Reaction Steps

This analog compound was obtained from reduction of N-[({3-acetyl-4-[7-fluoro-6-(methylamino)-1-oxoisoquinolin-2(1H)-yl]phenyl}amino)carbonyl]-5-chlorothiophene-2-sulfonamide of Example 70. To a solution of N-[({3-acetyl-4-[7-fluoro-6-(methylamino)-1-oxoisoquinolin-2(1H)-yl]phenyl}amino)carbonyl]-5-chlorothiophene-2-sulfonamide (18 mg, 0.033 mmol) in 2 mL ethanol, was added sodium borohydride (20 mg, 0.53 mmol). The mixture was stirred at room temperature for 30 minutes. Workup and purification provided 5-chloro-N-({[4-[7-fluoro-6-(methylamino)-1-oxoisoquinolin-2(1H)-yl]-3-(1-hydroxyethyl)phenyl]amino}carbonyl)thiophene-2-sulfonamide as a mixture of rotamers. ES-MS (M+H)+=551, 553(Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294635B2
Source datasetuspto-grants-2007_11
ORD IDord-eab5c27dccce43d7bedd4b1edda448e3
Source noteuspto-grants-2007_11