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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 22814775, 화합물 → HCID 53661776, 화합물

HRID 1414070
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HRID 1414070 반응식
C([N:11]1[CH2:18][C@H:17]([O:19][C:20]([NH:22][CH3:23])=[O:21])[CH2:16][C@H:12]1[C:13]([OH:15])=[O:14])(OCC1C=CC=CC=1)=O.[H][H]>[C].[Pd].CO.O>[CH3:23][NH:22][C:20]([O:19][C@H:17]1[CH2:18][NH:11][C@H:12]([C:13]([OH:15])=[O:14])[CH2:16]1)=[O:21]
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참가 물질

5

반응물 2

HCID 22814775HCID 22814775, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 53661776HCID 53661776, 화합물

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 22242641Methanol--water (1/1)용매

실험 절차

A solution of 2.7 g. (0.0084 mole) of trans-N-carbobenzyloxy-4-[[(methylamino)carbonyl]oxy]-L-proline in 100 ml. of methanol-water (2:1) is treated with 1 g. of 5% palladium-carbon and 45 lb. of hydrogen and shaken on a Parr hydrogenator for 6 hours. The catalyst is filtered off under nitrogen, washed with methanol and the combined filtrates are evaporated, finally at 0.1-0.2 mm, to give 1.5 g. (96%) of a residue which gradually crystallizes to give trans-4-[[(methylamino)carbonyl]oxy]-L-proline as a greyish solid; m.p. 213°-215° (dec.), preceded by gradual darkening and sintering. [α]D26 -12° (c, 0.25% in 1:3 ethanol-methanol).

후처리

  1. filtrationThe catalyst is filtered off under nitrogen
  2. washwashed with methanol
  3. customthe combined filtrates are evaporated, finally at 0.1-0.2 mm
  4. customto give 1.5 g
  5. custom(96%) of a residue which gradually crystallizes

출처 및 근거

ORD 기록
ord-472cda4926904690a05eb5e6fe4e8fee
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04252943

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