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Water → HCID 15381474, 화합물

HRID 2258117
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HRID 2258117 반응식
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
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참가 물질

8

반응물 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

생성물 1

HCID 15381474HCID 15381474, 화합물수율 92%

시약·촉매·용매 3

HCID 6212Chloroform용매HCID 6342Acetonitrile용매HCID 8857Ethyl Acetate용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-f9738477d84846a59c3d7f7e99d1ad22
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05659043

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