Stannous chloride dihydrate → HCID 21956071, 화합물

HRID 505435노트

반응식

HRID 505435 반응식
[NH2:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)=[CH:4][N:3]=1.O.O.Cl[Sn]Cl>C(O)C>[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([C:11]2[CH:12]=[CH:13][C:14]([F:17])=[CH:15][CH:16]=2)=[CH:4][N:3]=1

참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 219560765-(4-Fluorophenyl)-3-nitro-2-pyridinylamine

생성물 1

HCID 21956071HCID 21956071, 화합물수율 93.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 2.59 g of 2-amino-5-(4-fluorophenyl)-3-nitro-pyridine (compound G1) in 36 ml ethanol is treated with 12.9 g of SnCl2.2H2O at 90° C. for 24 h under a nitrogen atmosphere. Thereafter, the solution is concentrated to dryness. The residue is dissolved in 600 ml H2O and adjusted to pH 8 using a 1.0 M solution of aqueous sodium hydroxide. Subsequently, the aqueous layer is extracted six times each with 50 ml of ethyl acetate. The combined organic phases are extracted once with 100 ml of brine, dried using magnesium sulfate, filtered with suction, and evaporated to dryness to yield 2.12 g of the pure title compound of m.p. 261° C. MS: 204.3 (MH+). TLC: Rf=0.50 (dichloromethane/methanol 5:1).

후처리

  1. concentrationThereafter, the solution is concentrated to dryness
  2. dissolutionThe residue is dissolved in 600 ml H2O
  3. extractionSubsequently, the aqueous layer is extracted six times each with 50 ml of ethyl acetate
  4. extractionThe combined organic phases are extracted once with 100 ml of brine
  5. customdried
  6. filtrationfiltered with suction
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-fbd17e0aa7cf4f269e57bb73d953a2a5
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07781453B2

반응 노트

불러오는 중…