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Sulfuric Acid → 2-Piperidinecarboxylic acid, 5-[(phenylmethoxy)amino]-, phenylmethyl ester, (2S,5R)-

HRID 508458
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HRID 508458 반응식
[CH2:1]([O:8][C:9]([C@@H:11]1[CH2:16][CH2:15][C:14](=[N:17][O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:13][NH:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(=O)(=O)(O)O.[BH4-].[Na+]>O1CCCC1>[CH2:1]([O:8][C:9]([C@@H:11]1[CH2:16][CH2:15][C@@H:14]([NH:17][O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:13][NH:12]1)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 4311764Sodium borohydrideHCID 86702281Phenylmethyl (2S)-5-[(phenylmethoxy)imino]-2-piperidinecarboxylate

생성물 1

HCID 706739342-Piperidinecarboxylic acid, 5-[(phenylmethoxy)amino]-, phenylmethyl ester, (2S,5R)-수율 80%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-10 °C

실험 절차

Under nitrogen atmosphere, tetrahydrofuran (2 ml) was added to (2S)-5-benzyloxyimino-piperidine-2-carboxylic acid benzyl ester (0.168 g, 0.50 mmol), and the mixture was cooled down to −10° C. Sulfuric acid (0.302 g, 3.06 mmol) was added to the mixture, and then sodium borohydride (0.0567 g, 1.50 mmol) was added. After 22 hours of stirring, the reaction mixture was analyzed with high performance liquid chromatography to find that the mixture contained 0.136 g of the title compound, and the reduction reaction proceeded with the yield of 80%. The diastereo selectivity was (2S,5R)/(2S,5S)=80.4/19.6 (60.8% de).

출처 및 근거

ORD 기록
ord-7c4c08d5f923470a9f47d97d0bae6bb5
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096523B2

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