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Sodium borohydride → 3-{[(R)-1-(3-Fluorophenyl)ethylamino]-(4-methoxyphenyl)methyl}phenylamine

HRID 2269482
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HRID 2269482 반응식
[F:1][C:2]1[CH:3]=[C:4]([C@H:8]([NH:10][CH:11]([C:21]2[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[CH:23][CH:22]=2)[C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([N+:18]([O-])=O)[CH:13]=2)[CH3:9])[CH:5]=[CH:6][CH:7]=1.[BH4-].[Na+]>O.O.O.O.O.O.[Ni](Cl)Cl.CO>[F:1][C:2]1[CH:3]=[C:4]([C@H:8]([NH:10][CH:11]([C:21]2[CH:22]=[CH:23][C:24]([O:27][CH3:28])=[CH:25][CH:26]=2)[C:12]2[CH:13]=[C:14]([NH2:18])[CH:15]=[CH:16][CH:17]=2)[CH3:9])[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 70188098N-[(R)-1-(3-Fluorophenyl)ethyl]-N-[(4-methoxyphenyl)-(3-nitrophenyl)methyl]amine

생성물 1

HCID 701891533-{[(R)-1-(3-Fluorophenyl)ethylamino]-(4-methoxyphenyl)methyl}phenylamine

시약·촉매·용매 2

HCID 11791229Dichloronickel;hexahydrate촉매HCID 887Methanol용매

실험 절차

Following a similar procedure to that described in Example (59b), 15.08 g of N-[(R)-1-(3-fluorophenyl)ethyl]-N-[(4-methoxyphenyl)-(3-nitrophenyl)methyl]amine [prepared as described in step (a) above], 18.84 g of nickel chloride hexahydrate, 6.0 g of sodium borohydride and 150 ml of methanol were reacted, to obtain 787 mg and 605 mg of isomer A and isomer B of the title compound, respectively, each as a pale yellowish oil.

후처리

  1. customwere reacted

출처 및 근거

ORD 기록
ord-11dfe415ee3b490d88afe4cd970c2e1d
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06329405B1

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