Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578656Generated: October 29, 2026

Diisopropylethylamine → HCID 66762641, compound

https://huagongshe.com/reaction/578656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl [3-(1-aminoethyl)phenyl]carbamateHCID 16740731—
ReactantHCID 77231308HCID 77231308—
ProductHCID 66762641HCID 66762641—

Reaction Steps

To a solution of methyl 4,6-dichloroquinazoline-8-carboxylate (574 mg; 2.23 mmol; 1.00 eq.) in acetonenitrile (5 ml) containing N-ethyl-N-isopropylpropan-2-amine (0.80 ml; 4.47 mmol; 2.00 eq.) was added tert-butyl [3-(1-aminoethyl)phenyl]carbamate (543 mg; 2.30 mmol; 1.03 eq.), the reaction mixture was stirred at RT overnight. Concentrated to get 4-[1-(3-tert-butoxycarbonylamino-phenyl)-ethylamino]-6-chloro-quinazoline-8-carboxylic acid methyl ester. To this crude was added methanolic ammonia (3.19 ml; 7.00 M; 22.33 mmol; 10.00 eq.) and stirred at RT for 48 h. The solvent was removed and the residue, {3-[1-(8-Carbamoyl-6-chloro-quinazolin-4-ylamino)-ethyl]-phenyl}-carbamic acid tert-butyl ester was treated with 4.0M hydrogen chloride in dioxane (5.58 ml; 4.00 M; 22.33 mmol; 10.00 eq.) and methanol (6.45 ml). Stirred overnight, concentrated and purified by HPLC to collect the title product (130 mg) in 14% over all yield. MS (M+1) 342.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040560B2
Source datasetuspto-grants-2015_05
ORD IDord-2050b01abb804facaa747d7394a91e12
Source noteuspto-grants-2015_05