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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2259557생성일: 2026년 10월 27일

Dichloromethane → Calcitriol

https://huagongshe.com/reaction/2259557

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물2-Anilino-3-methyl-6-diethylaminofluoranHCID 122402—
반응물beta-CyclodextrinHCID 444041—
반응물AlfacalcidolHCID 5282181—
용매EthanolHCID 702—
생성물CalcitriolHCID 5280453—

반응 단계

Nocardia autotrophica N-102 in the same BG medium (100 ml/500 ml-Erlenmeyer flask) as used in Example 1 was cultured at 28° C. under the aerobic conditions for 48 hours. To the culture medium were added 10 ml of a 5% aqueous β-cyclodextrin solution (0.01 M phosphate buffer, pH 7.0), a solution of 1% 1-hydroxyvitamin D3 in 1 ml of ethanol (in the amount of 140 mol of β-cyclodextrin relative to 1 mol of 1α-hydroxyvitamin D3) and a solution of 20% Tween 80 in 1 ml of ethanol. After cultivation for a further 2 hours, methylene chloride was added to the flask, and the determination as described in Example 1 was carried out. The peak fraction having a retention time of 3.8 minutes was collected, concentrated to dryness at 40° C. or below under reduced pressure, and applied to HPLC on Zorbax ODS (made by Du Pont Co.) with water-methanol (1:9) as a mobile phase at a flow rate of 1.0 ml/min. After elution, the peak reaction having a retention time of 5.6 minutes was collected, and concentrated to dryness under pressure at 40° C. or below with a nitrogen gas replacement to give 645 μg (64.5% of conversion ratio from the material) of 1α,25-dihydroxyvitamin D3. In case of the same procedure as described above but without β-cyclodextrin, the yield was 350 μg (35% of the conversion ratio from the material).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05474923
출처 데이터셋uspto-grants-1995_12
ORD IDord-206bafe1ef3c4cff95dc27606e90b664
출처 메모uspto-grants-1995_12