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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238396Generated: October 30, 2026

Ammonia → 1-(chloromethyl)-7-cyano-5-nitro-1,2-dihydro-3H-benzo[e]indole

https://huagongshe.com/reaction/2238396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPotassium NitrateHCID 24434—
Reactanttert-butyl 1-(chloromethyl)-7-cyano-1,2-dihydro-3H-benzo[e]indole-3-carboxylateHCID 44550490—
SolventSulfuric AcidHCID 1118—
Product1-(chloromethyl)-7-cyano-5-nitro-1,2-dihydro-3H-benzo[e]indoleHCID 4454940162.6%

Reaction Steps

Powdered carbamate 143 (1.00 g, 2.9 mmol) was added portionwise to stirred conc. H2SO4 (10 mL) at 0° C., and the mixture was warmed to room temperature for 10 min. The resulting solution was cooled to −5° C. and treated dropwise with a solution of KNO3 (324 mg, 3.2 mmol) in cone. H2SO4 (2 mL). After siting for a flirter 5 min at 0° C., the mixture was poured into ice/water and neutralized with dilute aqueous NH3. The resulting solid was purified by chromatography on silica gel, eluting with CH2Cl2, followed by recrystallization from CH2Cl2, then EtOAc, to give 1-(chloromethyl)-7-cyano-5-nitro-1,2-dihydro-3H-benzo[e]indole (144) (522 mg, 62%) as a red solid: mp 237-238° C.; 1H NMR [(CD3)2SO] δ 8.55 (d, J=1.4 Hz, 1H), 7.98 (d, J=8.8 Hz, 1H), 7.77 (s, 1H), 7.74 (dd, J=8.8, 1.5 Hz, 1H), 6.87 (s, 1H), 4.29-4.21 (m, 1H), 3.94-3.85 (m, 2H), 3.80 (dd, J=11.1, 8.1 Hz, 1H), 3.75 (dd, J=10.6, 3.1 Hz, 1H). Anal. (C14H10ClN3O2) C, H, N, Cl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718688B2
Source datasetuspto-grants-2010_05
ORD IDord-16733de696af4bf68a33aece65ac4956
Source noteuspto-grants-2010_05