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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598855Generated: October 31, 2026

1,1,1-trimethyl-N-((trimethylsilyl)oxy)silylamine → N-((S)-3-(1H-indol-3-yl)-1-(3-(isoquinolin-6-yl)isoxazol-5-ylamino)propan-2-yl)-4-nitrobenzenesulfonamide

https://huagongshe.com/reaction/598855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-trimethyl-N-((trimethylsilyl)oxy)silylamineHCID 89815—
ReactantHCID 67062570HCID 67062570—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
ProductN-((S)-3-(1H-indol-3-yl)-1-(3-(isoquinolin-6-yl)isoxazol-5-ylamino)propan-2-yl)-4-nitrobenzenesulfonamideHCID 6706259086.2%

Reaction Steps

To a solution of allyl(S)-3-(1H-indol-3-yl)-2-(4-nitrophenylsulfonamido)propyl(3-(isoquinolin-6-yl)isoxazol-5-yl)carbamate (100 mg, 153 μmol) in 2.5 mL of DCM was added Pd(PPh3)4 (5.3 mg, 4.6 μmol) and N,O-bis(trimethylsilyl)hydroxylamine (27 mg, 153 μmol). The mixture was stirred for 15 minutes and was then quenched with 2.5 mL saturated aqueous NH4Cl and the biphasic mixture was stirred for 2 hours. The mixture was then partitioned and the aqueous portion was extracted twice with DCM. The combined organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by preparative LC to give N-((S)-3-(1H-indol-3-yl)-1-(3-(isoquinolin-6-yl)isoxazol-5-ylamino)propan-2-yl)-4-nitrobenzenesulfonamide (75 mg, 86% yield). MS m/z: 569 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-716ab312ebf94defb21729ae7ad86230
Source noteuspto-grants-2011_03