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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238419Generated: November 1, 2026

Ammonia → HCID 68695596, compound

https://huagongshe.com/reaction/2238419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium ChlorideHCID 5234—
ReactantN,N-DimethylethylenediamineHCID 66053—
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantHCID 68692459HCID 68692459—
SolventDimethylformamideHCID 6228—
ProductHCID 68695596HCID 6869559660%

Reaction Steps

A stirred solution of 187 (120 mg, 0.39 mmol) in dry DMF (1.5 mL) was treated at 0° C. with N,N-dimethyl-1,2-ethanediamine (107 μL, 0.97 mmol), followed by the dropwise addition of diethyl cyanophosphonate (128 μL, 93%, 0.78 mmol). The mixture was warmed to room temperature for 45 min, then poured into dilute aqueous NH3 saturated with NaCl. The resulting solid was collected, washed with water and recrystallised twice from CH2Cl2/i-Pr2O to give 1-(chloromethyl)-N-[2-(dimethylamino)ethyl]-5-nitro-1,2-dihydro-3H-benzo[e]indole-8-carboxamide (188) (88 mg, 60%) as a red solid: mp 178-180° C.; 1H NMR [(CD3)2SO] δ 8.68 (t, J=5.7 Hz, 1H), 8.22 (d, J=1.2 Hz, 1H), 8.16 (d, J=9.1 Hz, 1H), 7.77 (dd, J=9.1, 1.7 Hz, 1H), 7.72 (s, 1H), 6.41 (d, J=1.7 Hz, 1H), 4.28-4.18 (m, 1H), 3.98 (dd, J=10.9, 3.7 Hz, 1H), 3.84 (td, J=9.7, 2.4 Hz, 1H), 3.75 (dd, J=−11.0, 9.0 Hz, 2H), 3.49-3.37 (m, 2H), 2.45 (t, J=7.0 Hz, 2H), 2.21 (s, 6H). Anal. (C18H21ClN4O3) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718688B2
Source datasetuspto-grants-2010_05
ORD IDord-b14d10d1f8c0483a98bc27e67523c60c
Source noteuspto-grants-2010_05