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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Chloroform → HCID 86738946, 화합물

HRID 1074543
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HRID 1074543 반응식
[CH:1]([Cl:4])(Cl)Cl.[CH2:5]=[C:6]1[C@H:12]([CH3:13])[O:11]C(O)[CH2:8][C@@H:7]1[NH:14][C:15](=[O:20])[C:16]([F:19])([F:18])[F:17].FC(F)(F)C(OC(=O)C(F)(F)F)=O>C(Cl)Cl>[CH2:5]=[C:6]1[C@H:12]([CH3:13])[O:11][CH:1]([Cl:4])[CH2:8][C@@H:7]1[NH:14][C:15](=[O:20])[C:16]([F:18])([F:19])[F:17]
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참가 물질

5

반응물 3

HCID 6212ChloroformHCID 9845Trifluoroacetic anhydrideHCID 86738945HCID 86738945, 화합물

생성물 1

HCID 86738946HCID 86738946, 화합물수율 90%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 0.51 g (2 mmol) of the intermediate VIII in 10 ml of acetic acid and 40 ml of water was heated at 100° C. for two hours, then evaporated to dryness to give 2,3,4,6-tetradeoxy-4-C-methylene-3-trifluoroacetamido-L-threo-hexopyranose (IX, 0.47 g, 99%) as a white solid: m.p. 168°-170° C., [α]D20° -160° (c=0.5, CHCl3). Treatment of IX (0.36 g, 1.5 mmol) in 25 ml of dry methylene dichloride with 4 ml of trifluoroacetic anhydride for 2 hours at 0° C. and 1 hour at 20° C. gave, after evaporation, the 1-0-trifluoroacetate (X), which was directly used for the preparation of the corresponding 1-chloro-derivative by treatment with dry hydrogen chloride in anhydrous diethyl ether at 0° C. After standing at 0° C. overnight, the reaction mixture was evaporated to dryness to give 2,3,4,6-tetradeoxy-4-C-methylene-3-trifluoroacetamido-L-threo-hexopyranosyl chloride (III-A, 0.35 g, 90%), suitable for the subsequent coupling reaction without further purification.

후처리

  1. custom1 hour at 20° C. gave
  2. customafter evaporation
  3. customthe 1-0-trifluoroacetate (X), which was directly used for the preparation of the corresponding 1-chloro-derivative by treatment with dry hydrogen chloride in anhydrous diethyl ether at 0° C
  4. customthe reaction mixture was evaporated to dryness

출처 및 근거

ORD 기록
ord-94ec412498a04a35aa50efdb6e9f843b
출처 데이터셋
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04393052

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