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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720288Generated: October 28, 2026

Morpholine → HCID 69661871, compound

https://huagongshe.com/reaction/720288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantHCID 21060065HCID 21060065—
ProductHCID 69661871HCID 6966187130%

Reaction Steps

5-Benzyloxy-2-methanesulfonyl-1-methyl-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid ethyl ester (0.215 g, 0.58 mmol) was reacted with morpholine as described in the preparation of compound 1J. Chromatography on silica gel (elution toluene-ethyl acetate 8:2 to 6:4) gave first 0.050 g (30% yield) of 5-benzyloxy-1-methyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid ethyl ester as white crystals; mp 184–187° C. (ethyl acetate). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.34 (3H, t, J=7.1 Hz, CH3), 3.40 (3H, s, NCH3), 4.39 (2H, q, J=7.1 Hz, OCH2), 5.16 (3H, s, OCH2), 7.35–7.5 (5H, m, aromatics), 8.12 (1H, broad s, NH). Anal. Calcd for C15H16N2O5: C, 59.20; H, 5.30; N, 9.20. Found: C, 59.20; H, 5.08, N 9.19 . The end fractions then gave 0.102 g (47% yield) of the title ester as a white syrup. 1HNMR 400 MHz (CDCl3) δ (ppm): 1.29 (3H, t, J=7.1 Hz, CH3), 3.20 (4H, m, NCH2), 3.53 (3H, s, NCH3), 3.82 (4H, m, OCH2), 4.32 (2H, q, J=7.1 Hz, OCH2), 5.17 (2H, s, OCH2), 7.29–7.49 (5H, m, aromatics). HRMS (FAB POS) calculated for C19H24N3O5 [M+H+]: 374.171596. found: 374.1709485

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135467B2
Source datasetuspto-grants-2006_11
ORD IDord-ff98eb229e054760b27114917f72f306
Source noteuspto-grants-2006_11