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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421852Generated: November 1, 2026

Tert-Butylamine → HCID 25234371, compound

https://huagongshe.com/reaction/2421852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantHCID 86628747HCID 86628747—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 25234371HCID 2523437168.4%

Reaction Steps

To a biphasic mixture of 2,2-dimethyl-5-(phenylsulfonyl)-2,3,4,5-tetrahydrobenzo[b][1,4]thiazepine-7-carbonyl chloride (30 mg, 0.076 mmol) in DCM (2 mL) and saturated aqueous NaHCO3 (2 mL) was added tert-butylamine (25 μL, 0.236 mmol). The reaction was stirred at room temperature for 72 hours. TLC analysis of the reaction mixture indicated consumption of starting material. The biphasic mixture was extracted with DCM (3×2 mL). The combined organics were dried over Na2SO4 and concentrated in vacuo. The resulting solid was purified by flash column chromatography using a gradient elution of Hexanes with 5-50% EtOAc to provide N-tert-butyl-2,2-dimethyl-5-(phenylsulfonyl)-2,3,4,5-tetrahydrobenzo[b][1,4]thiazepine-7-carboxamide (26.3 mg, 0.052 mmol, 68.2% yield) as an off white solid. LCMS (+ESI) m/z=432.9 [M+H]+; 1H-NMR (CDCl3) δ 7.73-7.70 (m, 2H), 7.68-7.63 (m, 2H), 7.55 (tt, 1H), 7.49 (d, 1H), 7.47-7.41 (m, 2H), 5.89 (s, 1H), 3.77 (br s, 1H), 1.88 (br s, 2H), 1.46 (s, 9H), 1.12 (br s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960376B2
Source datasetuspto-grants-2011_06
ORD IDord-4af2f9540a5f49f9aba9a6935e5aa1d7
Source noteuspto-grants-2011_06