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Hydrochloric Acid → (E)-(S)-5-Amino-2-(3-fluoropropyl)hex-2-enedioic acid

HRID 1473721
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HRID 1473721 반응식
C(OC([NH:8][C@H:9]([C:22]([O:24]C(C)(C)C)=[O:23])[CH2:10]/[CH:11]=[C:12](\[CH2:18][CH2:19][CH2:20][F:21])/[C:13]([O:15]CC)=[O:14])=O)(C)(C)C.Cl>O>[NH2:8][C@H:9]([C:22]([OH:24])=[O:23])[CH2:10]/[CH:11]=[C:12](\[CH2:18][CH2:19][CH2:20][F:21])/[C:13]([OH:15])=[O:14]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 866784276-tert-Butyl 1-ethyl (E)-(S)-5-[(tert-butoxycarbonyl)amino]-2-(3-fluoropropyl)hex-2-enedioate

생성물 1

HCID 86678435(E)-(S)-5-Amino-2-(3-fluoropropyl)hex-2-enedioic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 6-tert-Butyl 1-ethyl (E)-(S)-5-[(tert-butoxycarbonyl)amino]-2-(3-fluoropropyl)hex-2-enedioate (1e) (80.0 mg, 0.20 mmol) and 4 N aqueous hydrochloric acid (1 mL) was heated to reflux for 4 h. The mixture was then cooled to r.t., diluted with water (5 mL) and lyophilised. The crude product was purified by preparative HPLC (XBridge C18, 5 μm 150×19 mm, acetonitrile/water (0.1% TFA) gradient, 21 mL/min). Yield: 12.0 mg, 0.04 mmol, 19%.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 4 h
  3. customThe crude product was purified by preparative HPLC (XBridge C18, 5 μm 150×19 mm, acetonitrile/water (0.1% TFA) gradient, 21 mL/min)

출처 및 근거

ORD 기록
ord-d786353c42d54b028e90030b8695df1b
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09017645B2

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