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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → N,N',N"-Tris[4-[[2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl)-beta-D-glucopyranosyl]oxy]phenyl]-1,3,5-benzenetrisulfonamide

HRID 1388312
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HRID 1388312 반응식
[C:1]([O:4][C@@H:5]1[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:17]([O:23][C@H:24]2[O:41][C@H:40]([CH2:42][O:43][C:44](=[O:46])[CH3:45])[C@@H:35]([O:36][C:37](=[O:39])[CH3:38])[C@H:30]([O:31][C:32](=[O:34])[CH3:33])[C@H:25]2[O:26][C:27](=[O:29])[CH3:28])[C@@H:16]([CH2:47][O:48][C:49](=[O:51])[CH3:50])[O:15][C@H:6]1[O:7][C:8]1[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][CH:9]=1)(=[O:3])[CH3:2].[C:52]1([S:66](Cl)(=[O:68])=[O:67])[CH:57]=[C:56]([S:58](Cl)(=[O:60])=[O:59])[CH:55]=[C:54]([S:62](Cl)(=[O:64])=[O:63])[CH:53]=1.[OH2:70]>N1C=CC=CC=1.C(#N)C.C(#N)C>[C:1]([O:4][C@@H:5]1[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:17]([O:23][C@H:24]2[O:41][C@H:40]([CH2:42][O:43][C:44](=[O:46])[CH3:45])[C@@H:35]([O:36][C:37](=[O:39])[CH3:38])[C@H:30]([O:31][C:32](=[O:34])[CH3:33])[C@H:25]2[O:26][C:27](=[O:29])[CH3:28])[C@@H:16]([CH2:47][O:48][C:49](=[O:51])[CH3:50])[O:15][C@H:6]1[O:7][C:8]1[CH:13]=[CH:12][C:11]([NH:14][S:66]([C:52]2[CH:57]=[C:56]([S:58]([NH:14][C:11]3[CH:10]=[CH:9][C:8]([O:70][C@@H:6]4[O:15][C@H:16]([CH2:47][O:48][C:49](=[O:51])[CH3:50])[C@@H:17]([O:23][C@H:24]5[O:41][C@H:40]([CH2:42][O:43][C:44](=[O:46])[CH3:45])[C@@H:35]([O:36][C:37](=[O:39])[CH3:38])[C@H:30]([O:31][C:32](=[O:34])[CH3:33])[C@H:25]5[O:26][C:27](=[O:29])[CH3:28])[C@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:5]4[O:4][C:1](=[O:3])[CH3:2])=[CH:13][CH:12]=3)(=[O:60])=[O:59])[CH:55]=[C:54]([S:62]([NH:14][C:11]3[CH:12]=[CH:13][C:8]([O:7][C@@H:6]4[O:15][C@H:16]([CH2:47][O:48][C:49](=[O:51])[CH3:50])[C@@H:17]([O:23][C@H:24]5[O:41][C@H:40]([CH2:42][O:43][C:44](=[O:46])[CH3:45])[C@@H:35]([O:36][C:37](=[O:39])[CH3:38])[C@H:30]([O:31][C:32](=[O:34])[CH3:33])[C@H:25]5[O:26][C:27](=[O:29])[CH3:28])[C@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:5]4[O:4][C:1](=[O:3])[CH3:2])=[CH:9][CH:10]=3)(=[O:64])=[O:63])[CH:53]=2)(=[O:68])=[O:67])=[CH:10][CH:9]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 889401,3,5-Benzenetrisulfonyl trichlorideHCID 132065724-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl)-beta-D-glucopyranoside

생성물 1

HCID 16162338N,N',N"-Tris[4-[[2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl)-beta-D-glucopyranosyl]oxy]phenyl]-1,3,5-benzenetrisulfonamide

시약·촉매·용매 2

HCID 6342Acetonitrile용매HCID 21959178Acetonitrile pyridine용매

실험 절차

To a solution of 2.45 g of 4-aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranoside in pyridine:acetonitrile (1:1) was added 440 mg of 1,3,5-benzenetrisulfonyl chloride in 2 ml of acetonitrile. The mixture was stirred overnight, then poured into 250 ml of water and filtered through diatomaceous earth. The filtrate was extracted with two 100 ml portions of ethyl acetate. The extracts were combined, washed with 100 ml of 1% hydrochloric acid, then 100 ml of brine, dried and filtered through hydrous magnesium silicate. This filtrate was evaporated to a solid residue which was purified by column chromatography on silica gel using a gradient system of hexane:ethyl acetate (1:1) to (1:3). Cuts of 250 ml were taken. Fractions 11-16 were combined, evaporated and crystallized from 50 ml of ethanol, giving 1.13 g of the desired intermediate as a white powder, mp 148°-151° C.

후처리

  1. filtrationfiltered through diatomaceous earth
  2. extractionThe filtrate was extracted with two 100 ml portions of ethyl acetate
  3. washwashed with 100 ml of 1% hydrochloric acid
  4. dry with material100 ml of brine, dried
  5. filtrationfiltered through hydrous magnesium silicate
  6. customThis filtrate was evaporated to a solid residue which
  7. customwas purified by column chromatography on silica gel using a gradient system of hexane:ethyl acetate (1:1) to (1:3)
  8. customevaporated
  9. customcrystallized from 50 ml of ethanol

출처 및 근거

ORD 기록
ord-8ae98af3532143f6b33a13a98f90a7a6
출처 데이터셋
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04431637

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