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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808459Generated: October 30, 2026

Diisopropylethylamine → 2-(3-(4-(1h-Indazol-5-ylamino)quinazolin-2-yl)phenoxy)-n-(cyanomethyl)acetamide

https://huagongshe.com/reaction/1808459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantAminoacetonitrile sulfate (1:1)HCID 196971—
ReactantPyBOPHCID 2724699—
Reactant2-(3-(4-((1H-indazol-5-yl)amino)quinazolin-2-yl)phenoxy)acetic acidHCID 59361988—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-(3-(4-(1h-Indazol-5-ylamino)quinazolin-2-yl)phenoxy)-n-(cyanomethyl)acetamideHCID 11950521—

Reaction Steps

A suspension of 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)acetic acid (70 mg, 0.14 mmol), PyBOP® (40 mg, 0.077 mmol), DIEA (24 μL, 0.14 mmol) in dry CH2Cl2:DMF (2:0.1 mL) was stirred at RT for 15 minutes. To this solution of activated acid was added aminoacetonitrile monosulfate (14 mg, 0.091 mmol). After 30 minutes, 1.0 equivalent of DIEA and 0.55 equivalents of PyBOP® were added. After stirring the solution for 15 minutes, 0.65 equivalents of aminoacetonitrile monosulfate were added and the mixture was stirred for an additional 30 minutes. The solvent was removed in vacuo and the crude product was purified using prep HPLC (15-40—90 mins) to afford 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(cyanomethyl)acetamide. (12 mg, 0.027 mmol, 19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357693B2
Source datasetuspto-grants-2013_01
ORD IDord-cdd1be66b3ce4e5881e974d98c6370f6
Source noteuspto-grants-2013_01