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Ethanol → HCID 68647310, 화합물

HRID 1162703
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HRID 1162703 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:12][C@@H:11]([O:13][CH3:14])[C@H:10]([C:15]#[N:16])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CC[OH:19]>C(Cl)(Cl)Cl.CC(O)=O.O=[Pt]=O>[C:11]([OH:13])(=[O:19])[CH3:12].[C:1]([O:5][C:6]([N:8]1[CH2:12][C@@H:11]([O:13][CH3:14])[C@H:10]([CH2:15][NH2:16])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 702EthanolHCID 58748311HCID 58748311, 화합물

생성물 1

HCID 68647310HCID 68647310, 화합물

시약·촉매·용매 3

HCID 345198Adams' catalyst촉매HCID 176Acetic Acid용매HCID 6212Chloroform용매

실험 절차

80.3 A suspension of (3S,4S)-3-cyano-4-methoxy-pyrrolidine-1-carboxylic acid tert-butyl ester (150 mg) in 15 ml of EtOH, 0.3 ml of chloroform, 0.38 ml of AcOH and 8 mg of PtO2 was hydrogenated at 22° C. and atmospheric pressure for 16 h. The suspension was filtered and the filtrate evaporated to give 188 mg of (3R,4S)-3-aminomethyl-4-methoxy-pyrrolidine-1-carboxylic acid tert-butyl ester acetate. Colorless semisolid. MS 231.3 ([M+H]+)

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후처리

  1. customwas hydrogenated at 22° C.
  2. filtrationThe suspension was filtered
  3. customthe filtrate evaporated

출처 및 근거

ORD 기록
ord-dcd9f4da7b824ed2981e9ccc2df3fac8
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820699B2

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