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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,1-trimethyl-N-((trimethylsilyl)oxy)silylamine | HCID 89815 | — |
| Reactant | HCID 67062570 | HCID 67062570 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-((S)-3-(1H-indol-3-yl)-1-(3-(isoquinolin-6-yl)isoxazol-5-ylamino)propan-2-yl)-4-nitrobenzenesulfonamide | HCID 67062590 | 86.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897619B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-716ab312ebf94defb21729ae7ad86230 |
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| Source note | uspto-grants-2011_03 |
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