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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162235Generated: October 29, 2026

1-(1,3-oxazol-2-ylmethyl)-1H-indazol-5-amine → (2R)-N,N-dimethyl-2-[(4-{[1-(1,3-oxazol-2-ylmethyl)-1H-indazol-5-yl]amino}quinazolin-5-yl)oxy]propanamide

https://huagongshe.com/reaction/1162235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1,3-oxazol-2-ylmethyl)-1H-indazol-5-amineHCID 68618912—
Reactant(2R)-N,N-dimethyl-2-[(4-oxo-3,4-dihydroquinazolin-5-yl)oxy]propanamideHCID 136346624—
Product(2R)-N,N-dimethyl-2-[(4-{[1-(1,3-oxazol-2-ylmethyl)-1H-indazol-5-yl]amino}quinazolin-5-yl)oxy]propanamideHCID 1611748280%

Reaction Steps

Using the same procedure as in Example 18, (2R)—N,N-dimethyl-2-[(4-oxo-3,4-dihydroquinazolin-5-yl)oxy]propanamide (212 mg, 0.81 mmol) and 1-(1,3-oxazol-2-ylmethyl)-1H-indazol-5-amine (1 equivalents) were reacted to give the title compound as a beige foam (295 mg, 80%); NMR spectrum (CDCl3) 1.73 (d, 3H), 3.06 (s, 3H), 3.14 (s, 3H), 5.43 (q, 1H), 5.71 (s, 2H), 6.81 (d, 1H), 7.09 (s, 1H), 7.48-7.53 (m, 2H), 7.58-7.62 (m, 2H), 7.88 (d, 1H), 8.07 (s, 1H), 8.41 (s, 1H), 8.61 (s, 1H), 10.92 (br s, 1H); Mass spectrum MH+ 458.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820683B2
Source datasetuspto-grants-2010_10
ORD IDord-9e716a937a74489f88fb2dc62150a388
Source noteuspto-grants-2010_10