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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263360생성일: 2026년 10월 26일

Carbon Dioxide → 3-(D-glucopyranos-6-yl)-1-(2-chloroethyl)-1-nitrosourea

https://huagongshe.com/reaction/263360

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Carbonic AcidHCID 767—
반응물D-GlucoseHCID 5793—
반응물GlyTouCan:G45127NYHCID 11008505—
반응물o-nitrophenyl N-(2-chloroethyl)N-nitrosocarbamateHCID 13231923—
용매Dimethyl SulfoxideHCID 679—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-(D-glucopyranos-6-yl)-1-(2-chloroethyl)-1-nitrosoureaHCID 2280812786.1%

반응 단계

1.79 g (10 mmol) of 6-amino-6-deoxy-D-glucopyranose is dissolved in a mixture of 20 ml anhydrous ethanol and 20 ml dimethyl sulfoxide, and the solution is cooled to 0°-5° C. To this solution is added 3.3 g (75 mmol) of dry-ice little by little so as to convert the glucopyranose into its carbonic acid-addition salt. This acid-addition salt solution is then added dropwise to a solution prepared by dissolving 3.28 g (12 mmol) of o-nitrophenyl N-(2-chloroethyl)N-nitrosocarbamate in a mixture of 40 ml anhydrous tetrahydrofuran and 10 ml toluene, while stirring, at 0°-5° C. over 30 minutes. The resultant mixture is stirred further at 20°-25° C. for 2 hours, and the thus reacted solution is concentrated at 40° C. and below, under reduced pressure. To the oily residue thus produced is added 80 ml of ethyl ether and the solution is left at 4° C. overnight. The crystalline residue obtained is washed with chloroform and then with ethyl ether, dried under reduced pressure, and recrystallized from anhydrous ethanol-n-hexane (4:1) to give 2.70 g of 3-(D-glucopyranos-6-yl)-1-(2-chloroethyl)-1-nitrosourea. Yield 86.1%. mp 102°-103° C. (decomp.). [α]D20 +55° (C 0.5, methanol; the value of +55° reduced to +37° after 18 hours). Analysis for C9H16N3O7Cl (MW 313.69):

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04156777
출처 데이터셋uspto-grants-1979_05
ORD IDord-e09bf44307fa45ea84f1ad4b6798682a
출처 메모uspto-grants-1979_05