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Citrulline → N-(2,3,4,5-tetrahydroxy-pentyl)-L-(+)-citrulline

HRID 438013
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HRID 438013 반응식
O=[CH:2][C@@H:3]([C@@H:5]([C@@H:7]([CH2:9][OH:10])[OH:8])[OH:6])[OH:4].[NH2:11][C@H:12]([C:20]([OH:22])=[O:21])[CH2:13][CH2:14][CH2:15][NH:16][C:17]([NH2:19])=[O:18]>[Ni]>[OH:4][CH:3]([CH:5]([OH:6])[CH:7]([OH:8])[CH2:9][OH:10])[CH2:2][NH:11][C@H:12]([C:20]([OH:22])=[O:21])[CH2:13][CH2:14][CH2:15][NH:16][C:17]([NH2:19])=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9750CitrullineHCID 5311110Aldehydo-D-ribose

생성물 1

HCID 54340382N-(2,3,4,5-tetrahydroxy-pentyl)-L-(+)-citrulline

시약·촉매·용매 1

HCID 935Nickel촉매

실험 절차

The product was made from D-ribose and L-(+)-citrulline using Raney nickel as a catalyst and heating for 2 hours to 50° C. and for 4 hours to 70° C. The product obtained had a melting point of 172° to 175° C. (decomposition) and an RF -value of 0.52 (determined as indicated under Example T).

후처리

  1. temperatureheating for 2 hours to 50° C. and for 4 hours to 70° C
  2. customThe product obtained

출처 및 근거

ORD 기록
ord-83b4416ca09743c682d22a1ff915884c
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04032676

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