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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536252Generated: October 30, 2026

2-aminopyrimidine-5-carboxylic Acid → HCID 178493864, compound

https://huagongshe.com/reaction/536252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-aminopyrimidine-5-carboxylic AcidHCID 7020367—
Reactant8-[3-(1,1-dioxo-1,4-thiazinan-4-yl)propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-amineHCID 178493865—
ProductHCID 178493864HCID 178493864—

Reaction Steps

The procedure used for the preparation of Example 16, Step 2 was used to prepare the title compound from 8-[3-(1,1-dioxidothiomorpholin-4-yl)propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine (Example 19, Step 1) and 2-aminopyrimidine-5-carboxylic acid. High vacuum drying at 60° C. gave the title compound (272 mg, 79%): HPLC MS RT=1.45 min, MH+=529.2; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 2.25-2.30 (2H, m), 3.44-3.49 (2H, m), 3.61-3.63 (4H, m), 3.83 (4H, bs), 3.99 (3H, s), 4.18-4.25 (2H, m), 4.33 (2H, t), 4.48-4.55 (2H, m), 7.43 (1H, d), 8.02 (1H, d), 9.04 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859572B2
Source datasetuspto-grants-2014_10
ORD IDord-78ef9f60311d4df2905460723a8dd63f
Source noteuspto-grants-2014_10