Organic Syntheses 2003
DOI: 10.1002/0471264180.os012.29
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Uramil

Abstract: Uramil product: uramil

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Cited by 1 publication
(2 citation statements)
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“…A solution of but-2-ynoic acid (801.0 mg, 9.52 mmol, 1.0 equiv), tert -butyl ( E )-(4-hydroxybut-2-en-1-yl)­carbamate (1.78 g, 9.52 mmol, 1.0 equiv), and DMAP (116.3 mg, 0.952 mmol, 0.1 equiv) in DCM (7.0 mL) was charged with DIC (1.5 mL, 9.62 mmol, 1.01 equiv). Additional but-2-ynoic acid (80.1 mg, 0.952 mmol, 0.1 equiv) was added after 50 min, and full consumption of alcohol was then observed.…”
Section: Methodsmentioning
confidence: 99%
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“…A solution of but-2-ynoic acid (801.0 mg, 9.52 mmol, 1.0 equiv), tert -butyl ( E )-(4-hydroxybut-2-en-1-yl)­carbamate (1.78 g, 9.52 mmol, 1.0 equiv), and DMAP (116.3 mg, 0.952 mmol, 0.1 equiv) in DCM (7.0 mL) was charged with DIC (1.5 mL, 9.62 mmol, 1.01 equiv). Additional but-2-ynoic acid (80.1 mg, 0.952 mmol, 0.1 equiv) was added after 50 min, and full consumption of alcohol was then observed.…”
Section: Methodsmentioning
confidence: 99%
“…A solution of 2,4,6-trichloro-5-nitropyrimidine (760.0 mg, 3.327 mmol, 1.0 equiv) was dissolved in DMF (20 mL) and cooled to −50 °C using a dry ice acetonitrile bath. Sodium tert -butoxide (639.1 mg, 6.655 mmol, 2.0 equiv) was added in portions, and the reaction was allowed to warm to room temperature over 45 min.…”
Section: Methodsmentioning
confidence: 99%