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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356258Generated: November 1, 2026

Sodium hydride → HCID 22396713, compound

https://huagongshe.com/reaction/1356258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-chloro-N,N-dimethylacetamideHCID 75886—
Reactanttert-butyl 1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylateHCID 22396759—
SolventDimethylformamideHCID 6228—
ProductHCID 22396713HCID 2239671390%

Reaction Steps

tert-Butyl 1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate (0.100 g, 0.349 mmol) was dissolved in DMF (1.0 mL) under N2 at rt. NaH (0.0450 g, 1.13 mmol, 3.22 equiv., 60% dispersion) was added and the mixture was stirred at rt for 30 min. 2-Chloro-N,N-dimethylacetamide (86 μL, 0.102 g, 0.838 mmol, 2.4 equiv.) was added, and the reaction mixture was stirred at rt for 24 h. The reaction mixture was poured over ice, then extracted with EtOAc (2×). The organic extracts was washed first with water, then with brine and dried over MgSO4. The organic extracts was filtered and concentrated to yield a crude product (0.148 g). The crude product was chromatographed (SiO2 18 g, eluted with 3:1 toluene:acetone) to give tert-butyl 6-[2-(dimethylamino)-2-oxoethyl]-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate (0.116 g) in 90% yield. 1H NMR (300 MHz, CDCl3) δ 1.50, 2.87-2.95, 3.01, 3.00-3.07, 3.13, 3.68-3.80, 4.85, 7.07-7.19, 7.47-7.51; MS (ESI+) for C21H29N3O3 m/z 372.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586421B2
Source datasetuspto-grants-2003_07
ORD IDord-b022b9cf817b4b0f8cdbe0b9b93c1445
Source noteuspto-grants-2003_07