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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853860Generated: October 30, 2026

Phenethylamine → HCID 58932539, compound

https://huagongshe.com/reaction/853860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantTetrahydrofuranHCID 8028—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3-Dioxoindoline-5-sulfonyl chlorideHCID 15908947—
SolventChloroformHCID 6212—
ProductHCID 58932539HCID 5893253915%

Reaction Steps

To a black solution of 2,3-Dioxo-2,3-dihydro-1H-indole-5-sulfonylchloride (4.00 g, 16.3 mmol) in 1:1 THF:CHCl3 was added, drop-wise via syringe pump, a solution of N-benzylmethylamine (2.73 mL, 21.2 mmol, 1.3 eq) and N,N-diisopropylethylamine (5.68 mL, 32.6 mmol, 2 eq) in CHCl3 (32 mL) over a period of 1.25 hr. with cooling in an ice bath. After stirring for 50 min. the reaction was allowed to warm to room temperature and stirred for 30 minutes. The reaction was concentrated. The crude product was purified on Biotage KP silica gel eluting with 98/2 CHCl2/CH3OH to give the analytically pure sample of the title compound as a bright yellow solid (0.18 g, 15% yield). Anal. Calc'd for C16H14N2O4S: C, 58.17; H, 4.27; N, 8.48. Found: C, 57.88; H, 4.36; N, 8.40. MS: (API-ES−) m/z 329 [M−H]. m.p.: 183-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256198B2
Source datasetuspto-grants-2007_08
ORD IDord-59e4b4742c8b421a92a46f61264fd923
Source noteuspto-grants-2007_08