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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267050Generated: November 3, 2026

1-Iodopropane → (6bR,10aS)-3-propyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline

https://huagongshe.com/reaction/1267050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
Reactantethyl (10R,15S)-3-oxo-1,4,12-triazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16)-triene-12-carboxylateHCID 20578971—
Product(6bR,10aS)-3-propyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxalineHCID 21302500—

Reaction Steps

Utilizing the material from Example 255 Step A, the title compound was prepared in analogous fashion using propyl iodide as the alkyl halide and following the procedure of Step B-D of Example 255, as an amorphous tan solid. 1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 2H), 1.40-2.01 (m, 6H), 2.65-2.70 (t, J=9.6 Hz, 2H), 2.70-2.95 (m, 2H), 2.95-3.45 (m, 7H)), 3.3.60-3.95 (m, 1H), 6.37(d, J=7.7 Hz, 1H), 6.46 (d, J=7.0 Hz, 1H), 6.64 (t, J=7.6 Hz) ppm. MS (CI): 258 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552017B1
Source datasetuspto-grants-2003_04
ORD IDord-6e67e81d4b224d508bf4c533baebaeba
Source noteuspto-grants-2003_04