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Formamide → HCID 178470647, 화합물

HRID 1503894
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HRID 1503894 반응식
[NH2:1][C:2]1[S:6][C:5]2[CH2:7][CH2:8][CH:9]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:4]=2[C:3]=1[C:16]([O:18]CC)=O.[CH:21]([NH2:23])=O>>[OH:18][C:16]1[C:3]2[C:4]3[CH:9]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:8][CH2:7][C:5]=3[S:6][C:2]=2[N:1]=[CH:21][N:23]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 713FormamideHCID 59379370ethyl 2-amino-4-(2-ethoxy-2-oxoethyl)-4H,5H,6H-cyclopenta[b]thiophene-3-carboxylate

생성물 1

HCID 178470647HCID 178470647, 화합물수율 43%

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온도
180 °C

실험 절차

To a 10-L 4-necked round-bottom flask, purged and maintained with an inert atmosphere of nitrogen, was added a solution of 15.2 (500 g, 1.68 mol, 1.00 equiv) in formamide (5 L) at room temperature. The resulting solution was stirred for 5 h at 180° C. in an oil bath. The reaction mixture was cooled to room temperature and then quenched by the addition of 10 L of water/ice. The resulting solution was extracted with 3×5 L of ethyl acetate and the organic layers were combined. The mixture was washed with 3×3000 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The solids were collected by filtration to afford 200 g (43%) of ethyl 2-[12-hydroxy-7-thia-9,11-diazatricyclo[6.4.0.0^[2,6]]dodeca-1(8),2(6),9,11-tetraen-3-yl]acetate (15.3) as a yellow solid.

후처리

  1. customTo a 10-L 4-necked round-bottom flask, purged
  2. temperaturemaintained with an inert atmosphere of nitrogen
  3. temperatureThe reaction mixture was cooled to room temperature
  4. customquenched by the addition of 10 L of water/ice
  5. extractionThe resulting solution was extracted with 3×5 L of ethyl acetate
  6. washThe mixture was washed with 3×3000 mL of brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated under vacuum
  9. filtrationThe solids were collected by filtration

출처 및 근거

ORD 기록
ord-33a1a2ce54cc4307ae09c2affed78d35
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09212190B2

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