Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162229Generated: October 28, 2026

1-(3-Fluorobenzyl)-1H-indazol-5-amine → (R)-2-(4-(1-(3-fluorobenzyl)-1H-indazol-5-ylamino)quinazolin-5-yloxy)-N,N-dimethylpropanamide

https://huagongshe.com/reaction/1162229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Fluorobenzyl)-1H-indazol-5-amineHCID 7147073—
Reactant(2R)-N,N-dimethyl-2-[(4-oxo-3,4-dihydroquinazolin-5-yl)oxy]propanamideHCID 136346624—
Product(R)-2-(4-(1-(3-fluorobenzyl)-1H-indazol-5-ylamino)quinazolin-5-yloxy)-N,N-dimethylpropanamideHCID 1611734874%

Reaction Steps

Using the same procedure as in Example 18, (2R)—N,N-dimethyl-2-[(4-oxo-3,4-dihydroquinazolin-5-yl)oxy]propanamide (200 mg, 0.77 mmol) and 1-(3-fluorobenzyl)-1H-indazol-5-amine (193 mg, 0.8 mmol) were reacted to give the title compound as a pale solid (272 mg, 74%); NMR Spectrum (CDCl3) 1.72 (d, 3H), 3.06 (s, 3H), 3.14 (s, 3H), 5.43 (q, 1H), 5.59 (s, 2H), 6.81 (d, 1H), 6.87 (d, 1H), 6.96 (m, 2H), 7.25 (m, 1H), 7.34 (d, 1H), 7.47 (d, 1H), 7.60 (t, 1H), 7.84 (dd, 1H), 8.07 (s, 1H), 8.42 (s, 1H), 8.62 (s, 1H); Mass spectrum 485.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820683B2
Source datasetuspto-grants-2010_10
ORD IDord-9d0f4a925a4c4b5d9236d2e3ce291081
Source noteuspto-grants-2010_10