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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408993Generated: October 30, 2026

3-Amino-5-tert-butylselenophene-2-carboxamide → HCID 86698308, compound

https://huagongshe.com/reaction/2408993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-5-tert-butylselenophene-2-carboxamideHCID 86646889—
ReactantDMF NaOHHCID 86698281—
ReactantHCID 86698307HCID 86698307—
ProductHCID 86698308HCID 86698308—

Reaction Steps

The reaction of 6-(3-morpholinopropoxy)-4-chloro-7-methoxy-2-methylquinazoline with 3-amino-5-tert-butylselenophene-2-carboxamide in the presence of DMF/NaOH as described in Example 1 gave title compound as a brown color solid, mp 204-206° C. 1H NMR (400 MHz, CDCl3): δ 11.92 (1H, br s), 8.95 (1H, s), 7.34 (1H, s), 7.18 (1H, s), 5.37 (2H, br s), 4.29 (2H, t, J=6.0 Hz), 3.98 (3H, s), 3.73 (4H, t, J=4.4 Hz), 2.70 (3H, s), 2.61 (2H, t, J=7.2 Hz), 2.50 (4H, br s), 2.11-2.14 (2H, m), 1.47 (9H, s); LC-MS (positive ion mode): m/z 560, 562 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815879B2
Source datasetuspto-grants-2014_08
ORD IDord-1589b5bc970d43d093f0219b46b9d262
Source noteuspto-grants-2014_08