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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167923Generated: October 31, 2026

Hydrochloric Acid → 5-Chloro-N4-(4-methoxyphenyl)-N4-methyl-9H-pyrimido[4,5-b]indole-2,4-diamine

https://huagongshe.com/reaction/2167923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantN-Methyl-4-anisidineHCID 22250—
ReactantHCID 45103998HCID 45103998—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
Product5-Chloro-N4-(4-methoxyphenyl)-N4-methyl-9H-pyrimido[4,5-b]indole-2,4-diamineHCID 5335907369%

Reaction Conditions

Temperature115 °C

Reaction Steps

To 10 (20 mg, 0.06 mmol) was added 4-methoxy-N-methyl aniline (61 mg, 0.44 mmol), 50 mL of Isopropanol, and 4 drops of cone. HCl in a 100 mL round bottom flask. The reaction mixture was refluxed at 110-120° C. for 26 hours, following which the Isopropanol was evaporated and the mixture was basified with ammonia in methanol to obtain a slight precipitate. The resulting precipitate was then dissolved in acetone and methanol. To the solution was added silica, and the solvent was removed under reduced pressure to provide a silica gel plug. The plug was transferred on top of a column packed with silica gel, twenty times the weight of plug, eluted with chloroform and 1% methanol in chloroform. Fractions containing the product AAG13 (TLC) were pooled and evaporated to give a solid which was further purified by washing with hexane. The overall yield was 69%. TLC Rf 0.25 (chloroform-methanol 20:1), m.p. 163-164° C., 1H NMR: δ 3.30 (s, 3H, OCH3), 3.66 (s, 3H, N—CH3), 6.55 (s, 2H, NH2, exch), 6.76-7.25 (m, 7H, ArH), 11.65 (s, 1H, 9-NH, exch). Anal. Calculated (C18H16ClN5O. 0.2 CH3(CH2)4—CH3): C, 62.15; H, 5.10; N, 18.87; Cl, 9.55. Found: C, 61.79; H, 4.95; N, 18.72; Cl, 9.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045489B2
Source datasetuspto-grants-2015_06
ORD IDord-b6939e9603244684b34da9ac34f6abb2
Source noteuspto-grants-2015_06