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phenylmethyl (2S)-2-(aminocarbonyl)-3,3-dimethyl-1-pyrrolidinecarboxylate → (S)-3,3-dimethylpyrrolidine-2-carboxamide

HRID 1014156
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HRID 1014156 반응식
[NH2:1][C:2]([C@@H:4]1[C:8]([CH3:10])([CH3:9])[CH2:7][CH2:6][N:5]1C(OCC1C=CC=CC=1)=O)=[O:3]>CO.[Pd]>[CH3:9][C:8]1([CH3:10])[CH2:7][CH2:6][NH:5][C@@H:4]1[C:2]([NH2:1])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 57878111phenylmethyl (2S)-2-(aminocarbonyl)-3,3-dimethyl-1-pyrrolidinecarboxylate

생성물 1

HCID 54083353(S)-3,3-dimethylpyrrolidine-2-carboxamide수율 102.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

In a 200 ml flask was dissolved phenylmethyl (2S)-2-(aminocarbonyl)-3,3-dimethyl-1-pyrrolidinecarboxylate (0.0192 mol, 5.3 g) in 80 ml methanol at 20° C. 10% Pd/C (Degussa type, 0.53 g) was added and the mixture was stirred for 5 hr under atmospheric H2. The catalyst was filtered and the reaction was concentrated yielding 2.8 g (quantitative) of 3,3-dimethyl-L-prolinamide as a white solid. LCMS (ESI+)=143 m/z (MH+). 1H NMR (400 MHz, CDCl3)— rotomers δ 7.20 (bs, 1H), 6.20 (bs, 1H), 3.32 (s, 1H), 3.05-3.01 (m, 2H), 2.50 (bs, 1H), 1.67-1.62 (m, 2H), 1.23 (s, 3H), 0.97 (s, 3H). [α]D +1.2° (c=0.5, methanol)

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후처리

  1. filtrationThe catalyst was filtered
  2. concentrationthe reaction was concentrated

출처 및 근거

ORD 기록
ord-f92d4124427b4fd1bc0dad2907108bc6
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07982053B2

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