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Hydromorphone Hydrochloride → Hydromorphone

HRID 17755
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인쇄 미리보기

반응식

HRID 17755 반응식
[CH3:1][N:2]1[C@@H:19]2[CH2:20][C:7]3=[CH:8][CH:9]=[C:10]([OH:21])[C:11]4[O:12][C@H:13]5[C:14]([CH2:16][CH2:17][C@@H:18]2[C@:5]5([C:6]=43)[CH2:4][CH2:3]1)=[O:15].Cl>O.[O-2].[O-2].[Ti+4]>[CH3:1][N:2]1[C@@H:19]2[CH2:20][C:7]3=[CH:8][CH:9]=[C:10]([OH:21])[C:11]4[O:12][C@H:13]5[C:14]([CH2:16][CH2:17][C@@H:18]2[C@:5]5([C:6]=43)[CH2:4][CH2:3]1)=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 5462347Hydromorphone Hydrochloride

생성물 1

HCID 5284570Hydromorphone

시약·촉매·용매 2

HCID 162651Titanium oxide (Ti3O)촉매HCID 962Water용매

실험 절차

Drug Loading. Hydromorphone beads were prepared by dissolving hydromorphone HCl in water, adding Opadry Y-5-1442, light pink (a product commercially available from Colorcon, West Point, Pa., which contains hydroxypropyl methylcellulose, hydroxypropyl cellulose, titanium dioxide, polyethylene glycol and D&C Red No. 30 aluminum lake) and mixing for about 1 hour to obtain a 20% w/w suspension. This suspension was then sprayed onto Nu-Pareil 18/20 mesh beads using a Wurster insert.

후처리

  1. additionadding Opadry Y-5-1442
  2. additionmixing for about 1 hour
  3. customto obtain a 20% w/w suspension

출처 및 근거

ORD 기록
ord-9c5f8a21995b459d9bee5dd6f95e8e97
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07740881B1

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