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Ammonium Chloride → 3-Bromo-N2-cyclopropyl-4-fluorobenzene-1,2-diamine

HRID 243138
ノート
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反応式

HRID 243138 の反応式
[Br:1][C:2]1[C:7](F)=[C:6]([N+:9]([O-])=O)[CH:5]=[CH:4][C:3]=1[F:12].CC[N:15]([CH:19]([CH3:21])[CH3:20])C(C)C.C1(N)CC1.[NH4+].[Cl-]>CC#N.[Fe]>[Br:1][C:2]1[C:3]([F:12])=[CH:4][CH:5]=[C:6]([NH2:9])[C:7]=1[NH:15][CH:19]1[CH2:21][CH2:20]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 25517Ammonium ChlorideHCID 69828CyclopropylamineHCID 81531DiisopropylethylamineHCID 137327452-Bromo-1,3-difluoro-4-nitrobenzene

生成物 1

HCID 681575913-Bromo-N2-cyclopropyl-4-fluorobenzene-1,2-diamine収率 62%

試薬・触媒・溶媒 2

HCID 23925Iron
触媒
HCID 6342Acetonitrile溶媒

実験手順

To a solution of 2-bromo-1,3-difluoro-4-nitrobenzene (1.19 g, 5.0 mmol) in MeCN (10 mL) were added DIPEA (1.74 mL, 10.0 mmol) and cyclopropylamine (360 mL, 5.17 mmol). The reaction mixture was stirred at RT for 4 h. The volatiles were removed under reduced pressure and the resulting residue was partitioned between DCM and water. The organic fraction was dried, concentrated in vacuo and the resulting residue taken up in a 3:1 mixture of MeOH:water (40 mL). NH4Cl (1.53 g, 28.6 mmol) and iron powder (1.06 g, 4.76 mmol) were added and the reaction mixture heated at 80° C. for 3 h. After cooling to RT, the mixture was filtered through a pad of Celite® and washed with additional MeOH. The filtrate was concentrated in vacuo and the resulting residue partitioned between DCM and an aqueous solution of NaHCO3. The organic fraction was dried and concentrated in vacuo and the resulting residue purified by column chromatography (Si—PCC, gradient 0-5% MeOH in EtOAc) to afford the title compound as a brown oil (759 mg, 62% over 2 steps). LCMS (Method C): RT 2.97 min [M+H]+ 245.02

後処理

  1. customThe volatiles were removed under reduced pressure
  2. customthe resulting residue was partitioned between DCM and water
  3. customThe organic fraction was dried
  4. concentrationconcentrated in vacuo
  5. additionthe resulting residue taken up in a 3:1 mixture of MeOH
  6. temperaturethe reaction mixture heated at 80° C. for 3 h
  7. temperatureAfter cooling to RT
  8. filtrationthe mixture was filtered through a pad of Celite®
  9. washwashed with additional MeOH
  10. concentrationThe filtrate was concentrated in vacuo
  11. customthe resulting residue partitioned between DCM
  12. customThe organic fraction was dried
  13. concentrationconcentrated in vacuo
  14. customthe resulting residue purified by column chromatography (Si—PCC, gradient 0-5% MeOH in EtOAc)

出典と根拠

ORDレコード
ord-d2d893eaeee54b598054e245e7a07920
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08653089B2

反応ノート

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