Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624546Generated: October 30, 2026

1-Methylpiperazine → HCID 136377200, compound

https://huagongshe.com/reaction/624546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 136377198HCID 136377198—
SolventDimethyl SulfoxideHCID 679—
SolventTolueneHCID 1140—
ProductHCID 136377200HCID 136377200—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 10-amino-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulene-7-carbonitrile hydrochloride, prepared as described in the previous step, (0.6 g) in DMSO (6 mL) and toluene (6 mL), was added 1-methylpiperazine (4 mL). The mixture was heated in a 130° C. oil bath for 17 hours. The solution was concentrated, diluted with ethyl acetate (50 mL), washed with water (20 mL) and brine (20 mL), and then concentrated. The solid was dissolved in dichloromethane (10 mL) and treated with saturated sodium bicarbonate solution. The title compound was collected as a light yellow precipitate, washed with water and dichloromethane, dried, and used in the next step without additional purification. LC-MS: m/z 338 (M+1). 1H NMR (CD3OD, 400 MHz): δ (ppm) 7.19-7.15 (m, 2H), 6.74 (d, 1H), 6.37 (s, 1H), 3.51 (m, 4H), 2.53 (m, 4H), 2.34 (s, 3H), 2.32 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303041B2
Source datasetuspto-grants-2016_04
ORD IDord-8703ad7d687d450092b3cd5af6ec396a
Source noteuspto-grants-2016_04