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HCID 86735596、化合物 → HCID 86735595、化合物

HRID 2082687
ノート
印刷プレビュー

反応式

HRID 2082687 の反応式
[CH2:1]([C@@:8]1([O:45][C@H:44]([CH2:46][O:47][C:48]([C:61]2[CH:66]=[CH:65][CH:64]=[CH:63][CH:62]=2)([C:55]2[CH:60]=[CH:59][CH:58]=[CH:57][CH:56]=2)[C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=2)[C@@H:39]([O:40][C:41](=[O:43])[CH3:42])[C@H:12]([O:13][CH2:14][C:15]([NH:17][C@H:18]([C:20]([NH:22][C@@H:23]([C:36](=[O:38])[NH2:37])[CH2:24][CH2:25][C:26]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[O:27])=[O:21])[CH3:19])=[O:16])[C@@:10]1([NH:67][C:68](=[O:70])[CH3:69])[OH:11])[OH:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)(=O)C>[CH2:1]([C@@:8]1([O:45][C@H:44]([CH2:46][OH:47])[C@@H:39]([O:40][C:41](=[O:43])[CH3:42])[C@H:12]([O:13][CH2:14][C:15]([NH:17][C@H:18]([C:20]([NH:22][C@@H:23]([C:36](=[O:38])[NH2:37])[CH2:24][CH2:25][C:26]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[O:27])=[O:21])[CH3:19])=[O:16])[C@@:10]1([NH:67][C:68](=[O:70])[CH3:69])[OH:11])[OH:9])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1.[CH2:1]([C@@:8]1([O:45][C@H:44]([CH2:46][O:47][C:48]([C:61]2[CH:62]=[CH:63][CH:64]=[CH:65][CH:66]=2)([C:55]2[CH:56]=[CH:57][CH:58]=[CH:59][CH:60]=2)[C:49]2[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=2)[C@@H:39]([O:40][C:41](=[O:43])[CH3:42])[C@H:12]([O:13][CH2:14][C:15]([NH:17][C@H:18]([C:20]([NH:22][C@@H:23]([C:36](=[O:38])[NH2:37])[CH2:24][CH2:25][C:26]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[O:27])=[O:21])[CH3:19])=[O:16])[C@@:10]1([NH:67][C:68](=[O:70])[CH3:69])[OH:11])[OH:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 86735596HCID 86735596、化合物

生成物 2

HCID 86735595HCID 86735595、化合物HCID 86735596HCID 86735596、化合物

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
100 °C

実験手順

A mixture of 0.94 g of benzyl (benzyl 2-acetamido-4-O-acetyl-6-O-triphenylmethyl-α-D-glucopyranosid-3-O-yl)acetyl-L-alanyl-D-isoglutaminate (12C, n = 2, X1 = L-alanyl, R2 = CH3, R3 = --COCH3) and 10 ml of 70% acetic acid is heated at a 100° C until a clear solution is obtained (about 2 minutes) and heating is contained for a further 2 minutes. The solution is immediately cooled in an ice bath and the precipitate is removed by filtration. The filtrate is evaporated to dryness in vacuo, the residue is triturated with 25 ml ether and the resultant solid is collected by filtration, washed with ether and dried in vacuo giving benzyl (benzyl 2-acetamido-4-O-acetyl-α-D-glucopyranosid-3-O-yl)acetyl-L-alanyl-D-isoglutaminate (12C, n = 2, X1 = L-alanyl, R2 = CH3, R3 = COCH3).

後処理

  1. customis obtained (about 2 minutes)
  2. temperatureheating
  3. temperatureThe solution is immediately cooled in an ice bath
  4. customthe precipitate is removed by filtration
  5. customThe filtrate is evaporated to dryness in vacuo
  6. customthe residue is triturated with 25 ml ether
  7. filtrationthe resultant solid is collected by filtration
  8. washwashed with ether
  9. customdried in vacuo

出典と根拠

ORDレコード
ord-a5b1bea9391a4ac0a9a1d777671f76b4
出典データセット
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04082735

反応ノート

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