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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716848Generated: October 30, 2026

Triethylamine → HCID 86689955, compound

https://huagongshe.com/reaction/716848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Nitrophenyl isocyanateHCID 76835—
Reactant1,4-Benzenediamine, N1,N1-bis(2-chloroethyl)-, hydrochloride (1:?)HCID 215727—
SolventChloroformHCID 6212—
ProductHCID 86689955HCID 86689955—

Reaction Steps

To a stirred mixture of N-mustard amine 18 (7.66 g, 25 mmol) and triethylamine (TEA, (4 mL, 27.5 mmol) in CHCl3 (100 mL) was added a solution of 3-nitrophenyl isocyanate 44a (4.1 g, 25 mmol) in CHCl3 (50 mL) dropwise at room temperature. After being stirred additional 40-45 minutes, the solvent was removed by evaporation under reduced pressure and the solid residue was triturated with saturated aqueous solution of NaHCO3 and then collected by filtration. The solid was washed with water, hexane, and dried. The solid was recrystallized from ethyl acetate to give 1-(4-(bis(2-chloroethyl)amino)phenyl)-3-(3-nitrophenyl)urea (45a), 9.1 g (92%); mp 246-247° C. 1H NMR (DMSO-d6) δ: 3.69-3.71 (8H, m, CH2), 6.71-6.74 (2H, d, J=9.0 Hz, Ar—H), 7.29-7.31 (2H, d, J=8.9 Hz, Ar—H), 7.52-7.56 (1H, t, J=8.1 and 8.2 Hz, Ar—H), 7.69-7.71 (1H, d, J=8.0 Hz, Ar—H), 7.78-7.80 (1H, q, J=8.2 and 1.8 Hz, Ar—H), 8.52 (1H, brs, NH), 8.54-8.55 (1H, d, J=2 Hz, Ar—H), 9.11 (1H, brs, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193687B2
Source datasetuspto-grants-2015_11
ORD IDord-caa95338fbaf42c9aeaf34608e64564d
Source noteuspto-grants-2015_11