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Ammonium Chloride → HCID 86727313, 화합물

HRID 518964
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HRID 518964 반응식
[CH3:1][CH:2]1[N:15]2[C:6]([CH2:7][O:8][C:9]3[C:14]2=[CH:13][C:12]([N+:16]([O-])=O)=[C:11]([CH3:19])[CH:10]=3)=[N:5][NH:4][C:3]1=[O:20].[Cl-].[NH4+]>CO.C1COCC1.[Zn]>[NH2:16][C:12]1[CH:13]=[C:14]2[C:9](=[CH:10][C:11]=1[CH3:19])[O:8][CH2:7][C:6]1[N:15]2[CH:2]([CH3:1])[C:3](=[O:20])[NH:4][N:5]=1
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참가 물질

6

반응물 2

HCID 25517Ammonium ChlorideHCID 86727312HCID 86727312, 화합물

생성물 1

HCID 86727313HCID 86727313, 화합물수율 79%

시약·촉매·용매 3

HCID 23994Zinc촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

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온도
70 °C

실험 절차

To a solution of 4,7-dimethyl-6-nitro-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (0.085 g, 0.31 mmol) and ammonium chloride (0.164 g, 3.1 mmol) in MeOH (10 mL) and THF (10 mL) was added zinc powder (0.200 g, 3.1 mmol) and the resulting mixture was heated at 70° C. for 4 h. The reaction mixture was cooled to ambient temperature, filtered and the filtrate was washed with MeOH (15 mL). The filtrate was concentrated in vacuo and the residue was dissolved in water (20 mL). The aqueous solution was extracted with EtOAc (3×15 mL) and the combined organic phase was dried over anhydrous Na2SO4, filtered and concentrated to give 6-amino-4,7-dimethyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (0.060 g, 0.24 mmol, 79%) as a solid, which was used directly in the next step. TLC (eluting with 25% EtOAc in petroleum ether) Rf=0.2.

후처리

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. filtrationfiltered
  3. washthe filtrate was washed with MeOH (15 mL)
  4. concentrationThe filtrate was concentrated in vacuo
  5. dissolutionthe residue was dissolved in water (20 mL)
  6. extractionThe aqueous solution was extracted with EtOAc (3×15 mL)
  7. dry with materialthe combined organic phase was dried over anhydrous Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a1b259be2de94d5d9447f38d094d3526
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115151B2

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