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HRID 81006作成日:2026年10月26日

Sodium Carbonate → (R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine 1-oxide

https://huagongshe.com/reaction/81006

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物Sodium ThiosulfateHCID 24477—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物(R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidineHCID 59670769—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物(R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine 1-oxideHCID 5811133753.1%

反応手順

m-CPBA (8.30 g, 37.0 mmol) was added in three portions to a solution of (R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine (2.5 g, 14.8 mmol) in CHCl3 (60 mL). The mixture was stirred at room temperature for 2 days. The mixture was cooled to 0° C., and Na2S2O3 (10 g) in water (60 mL) was added dropwise. Na2CO3 (6 g) in water (20 mL) was then added. The reaction mixture was stirred for 20 minutes. The aqueous phase was extracted with CHCl3 (2×200 mL), and the combined organic phases were concentrated at low temperature (<25° C.). The residue was purified by silica gel chromatography, eluting with ethyl acetate-DCM/MeOH (20:1) to give (R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine-oxide (1.45 g, 53%). 1H NMR (CDCl3, 400 MHz) δ 8.66 (s, 1H), 3.50 (m, 1H), 3.20 (m, 2H), 2.44 (m, 1H), 1.90 (m, 1H), 1.37 (d, J=7.2 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846683B2
出典データセットuspto-grants-2014_09
ORD IDord-59f388261ad44d5d8dcaf1f44d14253c
出典メモuspto-grants-2014_09