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HRID 4137作成日:2026年10月23日

Phosgene → 2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamide

https://huagongshe.com/ja/reaction/4137

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物Sulphonyl diisocyanateHCID 77898—
反応物2-Amino-4,6-dimethoxypyrimidineHCID 118946—
反応物2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamideHCID 13631887—
反応物2-(Chloromethyl)benzenesulfonyl isocyanateHCID 20152699—
触媒Diazabicyclo(2.2.2)octaneHCID 136165—
溶媒AcetonitrileHCID 6342—
溶媒O-XyleneHCID 7237—
生成物2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamideHCID 1336461769.6%

反応手順

A solution of 2-(chloromethyl)-N-(butylaminocarbonyl)benzene sulfonamide (1.33 g, 4.38 mmol) and diazabicyclo[2.2.2]octane (5 mg) in xylene (12 ml) was heated at reflux and contacted in portions with phosgene (1.0 ml. condensed phase). After 2.0 hrs at reflux, the mixture was cooled to room temperature, decanted, and volatiles were removed to give 1.56 g of crude product. The IR spectrum of 2-(chloromethyl)benzenesulfonyl isocyanate featured a strong band at 2250 cm-1. The crude sulfonyl isocyanate was contacted with acetonitrile (10 ml) and 2-amino-4,6-dimethoxypyrimidine (0.68 g, 4.4 mmol) and stirred for 16 hrs. Filtration gave 1.18 g of white solid, mp 192°-193°. The sample was dissolved in 0.5N NaOH, filtered and pH adjusted to 6.5. The mixture was cooled and filtered and the solid washed with ice water and dried to give 0.90 g of white solid. 1H nmr δDMSO-d6TMS 12.7 (brd s, 10.50 (s, 1H) 8.13-7.97 (m, 1H), 7.73-7.40 (m, 3H), 5.90 (s, 1H), 5.10 (s, 2H), 3.87 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723990
出典データセットuspto-grants-1988_02
ORD IDord-7101f12d796b4a7697ca6546a96de61b
出典メモuspto-grants-1988_02