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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → N-2-methyl-2-(methylthio)propanoyl-L-cysteine

HRID 127296
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HRID 127296 반응식
[NH2:1][C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][SH:4].[CH3:8][C:9]([S:14][CH3:15])([CH3:13])[C:10](Cl)=[O:11].Cl>C(=O)([O-])[O-].[K+].[K+]>[CH3:8][C:9]([S:14][CH3:15])([CH3:13])[C:10]([NH:1][C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][SH:4])=[O:11]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 5862L-(+)-CysteineHCID 134719922-Methyl-2-(methylthio)propanoyl chloride

생성물 1

HCID 53027N-2-methyl-2-(methylthio)propanoyl-L-cysteine수율 89.8%

시약·촉매·용매 1

HCID 11430Potassium Carbonate용매

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온도
0 °C

실험 절차

L-Cysteine (7.1 g) is dissolved in 88 ml of 2 M potassium carbonate and 7.5 g of 2-methyl-2-(methylthio)propanoyl chloride [b.p. 78° C. (37 mmHg)] is added dropwise while stirring under a nitrogen atmosphere at 0° C. After the addition, the mixture is stirred overnight at room temperature. The mixture is acidified with hydrochloric acid and the obtained crystals are separated by filtration and dried to yield 10.4 g (89.8%) of the titled compound.

후처리

  1. additionAfter the addition
  2. stirringthe mixture is stirred overnight at room temperature
  3. customthe obtained crystals are separated by filtration
  4. customdried

출처 및 근거

ORD 기록
ord-1ca328e86dbf4115a5c3fbcde3584ea3
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04255446

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