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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703174Generated: November 1, 2026

Triethylamine → HCID 13036382, compound

https://huagongshe.com/reaction/1703174

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-dimethoxy-quinazoline (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 IN 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 numberUS04351832
Source datasetuspto-grants-1982_09
ORD IDord-44a47055439f45b68a73cff8548c7038
Source noteuspto-grants-1982_09