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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156016Generated: November 1, 2026

Triethylamine → HCID 13036382, compound

https://huagongshe.com/reaction/1156016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-ChlorobenzothiazoleHCID 11987—
Reactant2-(1-Piperazinyl)-4-amino-6,7-dimethoxyquinazolineHCID 616267—
Solvent1-ButanolHCID 263—
ProductHCID 13036382HCID 13036382—

Reaction Steps

A suspension of 2-(1-piperazinyl)-4-amino-6,7-dimethoxyquinazoline (1.96 g), 2-chlorobenzthiazole (1.02 g), triethylamine (1.82 g) in butanol (100 ml) was refluxed for 72 hr and filtered. The precipitate was taken up in a solution of methanol and dimethyl sulfoxide, and 1 N sodium hydroxide was added until the mixture was alkaline. The precipitate was collected, washed with water, dried (1.3 g) and crystallized from methanol to give the title compound: mp 242°-245° C.; ir (nujol) 3460 and 3370 cm-1 : uv max (MeOH) 227 (ε=4130), 250 (ε=5280), 276 (ε=3649) and 340 nm (ε=690); nmr (DMSO-d6) δ 3.65 (m, 4H), 3.9 (m, 4H), 3.85 (s, 3H), 3.93 (s, 3H), 5.2 (s, 2H) and 7.2 (m, 6H); and Anal. Calcd for C21H22N6O2S.CH3OH: C, 58.14% H, 5.72% N, 18.50% and Found: C, 57.88% H, 5.90% N, 18.47%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04333937
Source datasetuspto-grants-1982_06
ORD IDord-b06d4efee8c94e6b9559755f8e934103
Source noteuspto-grants-1982_06