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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Glycine, N-methyl-, ethyl ester → HCID 86650566, 화합물

HRID 1746148
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HRID 1746148 반응식
Br[C:2]1[CH2:6][CH2:5][O:4][N:3]=1.NC1CCON=1.C([O:15][C:16](=[O:20])[CH2:17][NH:18][CH3:19])C>>[O:4]1[CH2:5][CH2:6][C:2]([N:18]([CH3:19])[CH2:17][C:16]([OH:20])=[O:15])=[N:3]1
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참가 물질

4

반응물 3

HCID 95849Glycine, N-methyl-, ethyl esterHCID 122690414,5-Dihydro-1,2-oxazol-3-amineHCID 219834983-Bromo-4,5-dihydroisoxazole

생성물 1

HCID 86650566HCID 86650566, 화합물

실험 절차

2-((4,5-dihydroisoxazol-3-yl)(methyl)amino)acetic acid I-244a and I-244b were prepared in 2 steps according to the following procedure: racemic 3-bromo-4,5-dihydroisoxazole I-10 was converted to the corresponding 3-amino-4,5-dihydroisoxazole by reacting it with sarcosine ethyl ester under the same conditions as in Example 238. The ethyl ester was then hydrolyzed using the analogous conditions as in Example 119 to provide a mixture of racemic I-244. These compounds can be separated using chiral HPLC methods known in the art. For example, see chiral HPLC Method disclosed herein. [M−H]−=327.5 m/z. Activity: B

후처리

  1. customto provide
  2. additiona mixture of racemic I-244
  3. customThese compounds can be separated

출처 및 근거

ORD 기록
ord-720be87f61ae411d956b5730c6ca5658
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09149465B2

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