Hydrazine hydrate (1:1) → 2-amino-7-aminomethyl-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid tert-butyl ester

HRID 965939

반응식

HRID 965939 반응식
[C:1]([O:5][C:6]([C:8]1[C:16]2[CH2:15][CH2:14][O:13][CH:12]([CH2:17][N:18]3C(=O)C4C(=CC=CC=4)C3=O)[C:11]=2[S:10][C:9]=1[NH2:29])=[O:7])([CH3:4])([CH3:3])[CH3:2].O.NN>C(O)C>[C:1]([O:5][C:6]([C:8]1[C:16]2[CH2:15][CH2:14][O:13][CH:12]([CH2:17][NH2:18])[C:11]=2[S:10][C:9]=1[NH2:29])=[O:7])([CH3:4])([CH3:2])[CH3:3]

참가 물질

4

실험 절차

To a mixture of 2-amino-7-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid tert-butyl ester (6.0 g, 0.014 mol) in ethanol (100 ml) was added hydrazine hydrate (1.4 ml, 0.028 mol). The reaction mixture was heated at reflux for 1 h, cooled and the precipitate filtered off. The filtrate was evaporated in vacuo and to the residue was added water (100 ml) and the resulting mixture was extracted with diethyl ether (2×100 ml). The combined organic extracts were washed with brine (100 ml), dried (Na2SO4), filtered and the solvent evaporated in vacuo affording 2.9 g (71%) of 2-amino-7-aminomethyl-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid tert-butyl ester as an oil.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 1 h
  3. temperaturecooled
  4. filtrationthe precipitate filtered off
  5. customThe filtrate was evaporated in vacuo and to the residue
  6. additionwas added water (100 ml)
  7. extractionthe resulting mixture was extracted with diethyl ether (2×100 ml)
  8. washThe combined organic extracts were washed with brine (100 ml)
  9. dry with materialdried (Na2SO4)
  10. filtrationfiltered
  11. customthe solvent evaporated in vacuo

출처 및 근거

ORD 기록
ord-f9db52eb2df449d69cfdffb8226365e5
출처 데이터셋
uspto-grants-2005_10
특허 번호
US06951878B2

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