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Sodium borohydride → HCID 18968908, 화합물

HRID 398786
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HRID 398786 반응식
[N:1]([CH:4]1[C:10](=[O:11])[NH:9][C:8]2[CH:12]=[CH:13][C:14]3[C:19]([C:7]=2[CH2:6][CH2:5]1)=[CH:18][CH:17]=[CH:16][CH:15]=3)=[N+]=[N-].[BH4-].[Na+]>C1COCC1.C(O)C>[NH2:1][CH:4]1[C:10](=[O:11])[NH:9][C:8]2[CH:12]=[CH:13][C:14]3[C:19]([C:7]=2[CH2:6][CH2:5]1)=[CH:18][CH:17]=[CH:16][CH:15]=3
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HCID 4311764Sodium borohydrideHCID 189689053-azido-4-oxo-2,3,4,5-tetrahydro-1H-naphtho[2,1-b]azepine

생성물 1

HCID 18968908HCID 18968908, 화합물

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 3-azido-4-oxo-2,3,4,5-tetrahydro-1H-naphtho[2, 1-b]azepine (1.0 g, 4.0 mmol) in dry THF (20 ml) was placed under an atmosphere of nitrogen and cooled by an ice-bath. A solution of sodium borohydride (0.17 g, 4.4 mmol) in ethanol (20 ml) was added dropwise during a period of 10 minutes and the reaction mixture was heated at reflux temperature for 20 h. The volatiles were evaporated in vacuo and the residue was purified by columm chromatography on silica gel (200 g) using dichloromethane and a mixture of ethanol and 25% NH3 (aq) (9:1) (gradient 0% to 10%) as eluent. This afforded 0.30 g of 3-amino-4-oxo-2,3,4,5-tetrahydro-1H-naphtho [2,1-b]azepine.

후처리

  1. temperaturecooled by an ice-bath
  2. temperaturethe reaction mixture was heated
  3. temperatureat reflux temperature for 20 h
  4. customThe volatiles were evaporated in vacuo
  5. customthe residue was purified by columm chromatography on silica gel (200 g)
  6. additiona mixture of ethanol and 25% NH3 (aq) (9:1) (gradient 0% to 10%) as eluent

출처 및 근거

ORD 기록
ord-196b4b9eba7c4e99b56241f2a3145270
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05817654

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