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3-Chloro-4,4-diethoxybutan-2-one → HCID 89662793, 화합물

HRID 1479046
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HRID 1479046 반응식
C(OC([N:8]1[CH2:15][C:14]2[C:10](=[N:11][NH:12][C:13]=2[NH2:16])[CH2:9]1)=O)(C)(C)C.[Cl:17][CH:18]([CH:22](OCC)OCC)[C:19](=O)[CH3:20]>CC(O)=O>[Cl:17][C:18]1[C:19]([CH3:20])=[N:16][C:13]2[N:12]([N:11]=[C:10]3[CH2:9][NH:8][CH2:15][C:14]3=2)[CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 127217263-Chloro-4,4-diethoxybutan-2-oneHCID 178451527HCID 178451527, 화합물

생성물 1

HCID 89662793HCID 89662793, 화합물수율 31.5%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A solution of 3-amino-2,6-dihydro-4H-pyrrolo[3,4-c]pyrazole-5-carboxylic acid tert-butyl ester (5.8 g; 25.9 mmol; 1 eq.) and 3-chloro-4,4-diethoxy-butan-2-one (5.6 g; 25.9 mmol; 1 eq.) in AcOH (26 mL) was stirred at room temperature for 16 hours then concentrated in vacuo. The residue was poured onto sat. aq. NaHCO3 and the formed precipitate was filtered off and dried. Purification by column chromatography (30% EA in heptane) afforded the title compound (1.7 g, 22%) as a white solid. 1H NMR (DMSO-d6) δ 9.48 (s, 1H), 4.62-4.54 (m, 4H), 2.60-2.57 (m, 3H), 1.48 (s, 9H). HPLC (max plot) 97.0%, Rt 3.93 min. UPLC/MS: (MS+) 309.3 ([M+H]+).

후처리

  1. concentrationthen concentrated in vacuo
  2. additionThe residue was poured onto sat. aq. NaHCO3
  3. filtrationthe formed precipitate was filtered off
  4. customdried
  5. customPurification by column chromatography (30% EA in heptane)

출처 및 근거

ORD 기록
ord-04d8eba4c7d94cfdbd8180891b6dc24d
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09403835B2

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