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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443008Generated: November 1, 2026

Glycolic Acid → (3R,5S)-5-[({4-[3-Chloro-4-fluoroanilino]-7-methoxyquinazolin-5-yl}oxy)methyl]1-glycoloylpyrrolidin-3-ol

https://huagongshe.com/reaction/1443008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycolic AcidHCID 757—
Reactant(3R,5S)-5-[({4-[3-chloro-4-fluoroanilino]-7-methoxyquinazolin-5-yl}oxy)methyl]pyrrolidin-3-olHCID 68675709—
Product(3R,5S)-5-[({4-[3-Chloro-4-fluoroanilino]-7-methoxyquinazolin-5-yl}oxy)methyl]1-glycoloylpyrrolidin-3-olHCID 5871072853%

Reaction Steps

The procedure described in Example 20 was repeated using (3R,5S)-5-[({4-[3-chloro-4-fluoroanilino]-7-methoxyquinazolin-5-yl}oxy)methyl]pyrrolidin-3-ol (209 mg) with glycolic acid (42 mg) to give the title compound as a white solid in 53% yield; NMR spectrum (DMSO-d6) 10.17 (s, 1H), 8.53 (s, 1H), 8.14 (dd, 1H), 7.74-7.69 (m, 1H), 7.47 (t, 1H), 6.92 (d, 1H), 6.83 (d, 1H), 5.14-5.10 (m, 1H), 4.71-4.67 (m, 1H), 4.50-4.44 (m, 1H), 4.40-4.38 (m, 1H), 4.28-4.23 (m, 1H), 4.06-4.03 (m, 2H), 3.95 (s, 3H), 3.53-3.48 (m, 3H), 2.05-2.02 (m, 2H); Mass spectrum MH+ 477.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659279B2
Source datasetuspto-grants-2010_02
ORD IDord-a00ed94268b448db8b68729c4ac9b758
Source noteuspto-grants-2010_02