ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Water → HCID 15381474、化合物

HRID 2258117
ノート
印刷プレビュー

反応式

HRID 2258117 の反応式
Cl.[SH:2][CH:3]1[CH2:6][N:5]([C:7]2[S:8][CH2:9][CH2:10][N:11]=2)[CH2:4]1.O.C1(P(O[C:28]2[C@H:29]([CH3:52])[C@@H:30]3[C@@H:47]([C@H:48]([OH:50])[CH3:49])[C:46](=[O:51])[N:31]3[C:32]=2[C:33]([O:35][CH2:36][C:37]2[CH:42]=[CH:41][C:40]([N+:43]([O-:45])=[O:44])=[CH:39][CH:38]=2)=[O:34])(C2C=CC=CC=2)=O)C=CC=CC=1.C(N(C(C)C)CC)(C)C>C(OC(=O)C)C.C(Cl)(Cl)Cl.C(#N)C>[S:8]1[CH2:9][CH2:10][N:11]=[C:7]1[N:5]1[CH2:6][CH:3]([S:2][C:28]2[C@H:29]([CH3:52])[C@@H:30]3[C@@H:47]([C@H:48]([OH:50])[CH3:49])[C:46](=[O:51])[N:31]3[C:32]=2[C:33]([O:35][CH2:36][C:37]2[CH:38]=[CH:39][C:40]([N+:43]([O-:45])=[O:44])=[CH:41][CH:42]=2)=[O:34])[CH2:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 962WaterHCID 81531DiisopropylethylamineHCID 119748831-(4,5-Dihydro-1,3-thiazol-2-yl)azetidine-3-thiol--hydrogen chloride (1/1)HCID 15871605p-nitrobenzyl (1R,5R,6S)-2-(di-phenylphosphoryloxy)-6-[(R)-1-hydroxyethyl]-1-methyl-carbapen-2-em-3-carboxylate

生成物 1

HCID 15381474HCID 15381474、化合物収率 92%

試薬・触媒・溶媒

3
HCID 6212Chloroform溶媒HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒

実験手順

There was dissolved 700 mg of 3-mercapto-1-(1,3-thiazolin-2-yl)azetidine hydrochloride (8), which was obtained in the above Example 6, in 15 ml of a mixed solvent composed of water, acetonitrile and chloroform, and, to the resulting solution, there was added 1668 mg of p-nitrobenzyl (1R,5R,6S)-2-(diphenylphosphoryloxy)-6-[(R)-1-hydroxyethyl]-1-methyl-carbapen-2-em-3-carboxylate (14). To the obtained solution which was being cooled with ice, there was added 2.8 ml of diisopropylethylamine in the stream nitrogen, and the resulting mixture was stirred at the same temperature for two hours. To the reaction liquid, there was added ethylacetate, and the resulting solution was washed with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, and, then, the solvent was evaporated in a vacuum, and the obtained residue was subjected to silica gel column chromatography (eluent: chloroform-acetone), and, thus, there was produced 1339 mg (yield: 92%) of p-nitrobenzyl (1R,5S,6S)-2-[1-(1,3-thiazolin-2-yl)azetidin-3-yl]thio-6-[(R)-1-hydroxyethyl]-1-methyl-carbapen-2-em-3-carboxylate (15).

後処理

  1. temperatureTo the obtained solution which was being cooled with ice, there
  2. customTo the reaction liquid, there
  3. washthe resulting solution was washed with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride
  4. customthe solvent was evaporated in a vacuum

出典と根拠

ORDレコード
ord-f9738477d84846a59c3d7f7e99d1ad22
出典データセット
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05659043

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート