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Sodium borohydride → HCID 59186059, 화합물

HRID 1671345
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HRID 1671345 반응식
[BH4-].[Na+].[Cl:3][C:4]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:5]=1[C:11]1[N:12]2[N:19]=[C:18]([CH3:20])[C:17]([N+:21]([O-])=O)=[C:13]2[O:14][C:15]=1[CH3:16]>CO.B#[Ni].O.O.O.O.O.O.[Ni](Cl)Cl>[Cl:3][C:4]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:5]=1[C:11]1[N:12]2[N:19]=[C:18]([CH3:20])[C:17]([NH2:21])=[C:13]2[O:14][C:15]=1[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 4311764Sodium borohydride2회HCID 67212560HCID 67212560, 화합물

생성물 1

HCID 59186059HCID 59186059, 화합물

시약·촉매·용매 3

HCID 82791nickel boride (NiB)촉매HCID 11791229Dichloronickel;hexahydrate촉매HCID 887Methanol용매2회

실험 절차

To a stirred suspension of black nickel boride (prepared in situ from 0.50 g, 2.15 mmol nickel (II) chloride hexahydrate and (0.080 g, 2.15 mmol sodium borohydride) in MeOH (15 ml) at RT is added a solution of 3-(2,4-dichloro-phenyl)-2,6-dimethyl-7-nitro-pyrazolo[5,1-b]oxazole (1.40 g, 4.29 mmol) in MeOH (55 ml). Further sodium borohydride (0.74 g, 19.5 mmol) is added in portions and the reaction is stirred at RT for 1 hour. The reaction is quenched by the addition of water (200 ml) and reduced in vacuo to remove the MeOH. EtOAc is added and the mixture passed through a Celite® (filter material) 521 pad. The crude product is extracted with EtOAc (2×125 ml) and the combined extracts are then extracted using 0.2N HCl (2×120 ml). The aqueous portions are combined and basified with 1N NaOH to pH10 to yield the title compound as a solid, which is filtered off and dried in vacuo; MS: m/z 296.1 [M+H]+

후처리

  1. customThe reaction is quenched by the addition of water (200 ml)
  2. customto remove the MeOH
  3. additionEtOAc is added
  4. filtrationthe mixture passed through a Celite® (filter material) 521 pad
  5. extractionThe crude product is extracted with EtOAc (2×125 ml)
  6. extractionthe combined extracts are then extracted

출처 및 근거

ORD 기록
ord-2336220c469f49c689cff1bfd0653d44
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994203B2

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