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Hydrochloric Acid → HCID 58095730, 화합물

HRID 2066797
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반응식

HRID 2066797 반응식
Cl.[CH3:2][C:3]1[N:4]=[C:5]([NH:20]C(=O)C)[S:6][C:7]=1[C:8]1[N:9]=[C:10]([C:13]2([C:16]([F:19])([F:18])[F:17])[CH2:15][CH2:14]2)[S:11][CH:12]=1>CCO>[CH3:2][C:3]1[N:4]=[C:5]([NH2:20])[S:6][C:7]=1[C:8]1[N:9]=[C:10]([C:13]2([C:16]([F:19])([F:18])[F:17])[CH2:14][CH2:15]2)[S:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86649582HCID 86649582, 화합물

생성물 1

HCID 58095730HCID 58095730, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

HCl (1.17 g 32% aqueous solution) was added to a solution of N-[4′-methyl-2-(1-trifluoromethyl-cyclopropyl)-[4,5′]bithiazolyl-2′-yl]-acetamide (Step 10.3) (0.18 g) in EtOH (10 mL) and the reaction mixture heated at reflux for 7 h. The cooled reaction mixture was partitioned between EtOAc and aqueous NaHCO3 solution, the organic layers dried over Na2SO4 and evaporated to give the title compound. MS (ESI): positive 306.1 (M+H), negative 304.1 (M−H).

후처리

  1. temperaturethe reaction mixture heated
  2. temperatureat reflux for 7 h
  3. customThe cooled reaction mixture
  4. customwas partitioned between EtOAc and aqueous NaHCO3 solution
  5. dry with materialthe organic layers dried over Na2SO4
  6. customevaporated

출처 및 근거

ORD 기록
ord-6ba4be43f7d246b28a856a1349659a3a
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08293753B2

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