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Bicarbonate Ion → (2-Amino-thiazol-5-yl)-propynoic acid ethyl ester

HRID 1889182
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반응식

HRID 1889182 반응식
[CH2:1]([O:3][C:4](=[O:20])[C:5]#[C:6][C:7]1[S:11][C:10]([NH:12]C(OC(C)(C)C)=O)=[N:9][CH:8]=1)[CH3:2].FC(F)(F)C(O)=O.C(=O)(O)[O-]>C(Cl)Cl>[CH2:1]([O:3][C:4](=[O:20])[C:5]#[C:6][C:7]1[S:11][C:10]([NH2:12])=[N:9][CH:8]=1)[CH3:2]
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참가 물질

5

반응물 3

HCID 769Bicarbonate IonHCID 6422Trifluoroacetic acid2회HCID 59610061(2-Tert-butoxycarbonylamino-thiazol-5-yl)-propynoic acid ethyl ester

생성물 1

HCID 59610026(2-Amino-thiazol-5-yl)-propynoic acid ethyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(2-tert-Butoxycarbonylamino-thiazol-5-yl)-propynoic acid ethyl ester (1.2 g, 4.049 mmol) was dissolved in DCM (20 ml), trifluoroacetic acid (4.617 g, 40.93 mmol) was added in drop wise fashion at 0° C. After complete addition the reaction was allowed to stir for overnight at room temperature. Additional 3 ml of TFA was charged to the reaction and stirred for 2 hr. TLC showed complete reaction. Reaction was basified with sat. bicarbonate. The aqueous layer was extracted with ethyl acetate (30 ml×3). The combined organic layer was washed with water followed by brine and dried over anhydrous sodium sulfate and the solvent was removed on vacuo. The sticky solid product was obtained (0.700 g)

후처리

  1. additionAfter complete addition the reaction
  2. stirringstirred for 2 hr
  3. customreaction
  4. customReaction
  5. extractionThe aqueous layer was extracted with ethyl acetate (30 ml×3)
  6. washThe combined organic layer was washed with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. customthe solvent was removed on vacuo
  9. customThe sticky solid product was obtained (0.700 g)

출처 및 근거

ORD 기록
ord-8d2d2c20bd6b45f4919e12247acbfbe3
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501955B2

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