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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
ノート
印刷プレビュー

反応式

HRID 1388312 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 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

生成物 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

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 21959178Acetonitrile pyridine溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8ae98af3532143f6b33a13a98f90a7a6
出典データセット
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04431637

反応ノート

読み込み中…

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