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Trifluoroacetic acid methylene chloride → (2S,3R)-2-amino-3-azido-butyric acid methylester hydrochloride

HRID 1692508
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HRID 1692508 반응식
[CH3:1][O:2][C:3](=[O:30])[C@@H:4]([NH:10]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[C@H:5]([N:7]=[N+:8]=[N-:9])[CH3:6].C(O)(C(F)(F)F)=O.C(Cl)[Cl:39]>Cl>[ClH:39].[CH3:1][O:2][C:3](=[O:30])[C@@H:4]([NH2:10])[C@H:5]([N:7]=[N+:8]=[N-:9])[CH3:6]
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참가 물질

4

반응물 2

HCID 21863450Trifluoroacetic acid methylene chlorideHCID 59697069(2S,3R)-methyl 3-azido-2-(tritylamino)butanoate

생성물 1

HCID 86643747(2S,3R)-2-amino-3-azido-butyric acid methylester hydrochloride수율 97%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A solution of Trt-Azido-Thr-OMe (3) (4.8 g, 12.0 mmol) was dissolved in a 95% TFA/DCM solution (60 ml) at rt with stirring. After 2.5 h, the reaction was complete by LCMS. The bright yellow solution was diluted with 0.5 N aq. HCl (300 ml). The aqueous layer was extracted with DCM (2×30 ml) and then lyophilized to dryness. The white solid was dissolved in AcCN/water (50:50) (100 ml) and again lyophilized to dryness to produce a consistent powder and remove as much of the TFA as possible. The azido-Thr product (4), 2.26 g (97% yield, 95% pure) of a white solid, was obtained as the HCl salt.

후처리

  1. extractionThe aqueous layer was extracted with DCM (2×30 ml)
  2. dissolutionThe white solid was dissolved in AcCN/water (50:50) (100 ml)
  3. customto produce a consistent powder
  4. customremove as much of the TFA as possible

출처 및 근거

ORD 기록
ord-1e0ec3529539430c81a0cbaaa63930b8
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153843B2

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