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Methylamine → HCID 59253237, 화합물

HRID 386891
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HRID 386891 반응식
[C:1]([O:5][C:6](=[O:18])[NH:7][C:8]1[O:12][N:11]=[C:10]([C:13]([CH3:17])([CH3:16])[CH:14]=O)[CH:9]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:19][NH2:20].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C>C1COCC1>[C:1]([O:5][C:6](=[O:18])[NH:7][C:8]1[O:12][N:11]=[C:10]([C:13]([CH3:17])([CH3:16])[CH2:14][NH:20][CH3:19])[CH:9]=1)([CH3:4])([CH3:3])[CH3:2]
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5

반응물 3

HCID 6329MethylamineHCID 2724942TriacetoxyborohydrideHCID 59253218[3-(1,1-Dimethyl-2-oxo-ethyl)-isoxazol-5-yl]-carbamic acid tert-butyl ester

생성물 1

HCID 59253237HCID 59253237, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

[3-(1,1-Dimethyl-2-oxo-ethyl)-isoxazol-5-yl]-carbamic acid tert-butyl ester (150.0 mg, 0.59 mmol) is dissolved in THF (1.0 mL) and 2M methylamine in THF (0.35 mL, 0.71 mmol) is added followed by the addition of MP-triacetoxyborohydride (546.0 mg, 2.70 mmol/g). The reaction mixture is placed on a shaker for 2 h. After this time, the reaction mixture is filtered and the filtrate is concentrated under reduced pressure to provide 163.0 mg of the title compound which is used crude for the next step. m/z 270 [M+H].

후처리

  1. filtrationAfter this time, the reaction mixture is filtered
  2. concentrationthe filtrate is concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-760c7d9c02804376b3233a31443e66cb
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372874B2

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