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Ammonia → 5-[({[3'-(aminomethyl)biphenyl-4-yl]methyl}sulfonyl)methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

HRID 606517
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HRID 606517 반응식
[O:1]=[C:2]1[NH:6][N:5]=[C:4]([CH2:7][S:8]([CH2:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]3[CH:23]=[CH:22][CH:21]=[C:20]([C:24]#[N:25])[CH:19]=3)=[CH:14][CH:13]=2)(=[O:10])=[O:9])[NH:3]1.N.CO>C1COCC1.[Ni]>[NH2:25][CH2:24][C:20]1[CH:19]=[C:18]([C:15]2[CH:16]=[CH:17][C:12]([CH2:11][S:8]([CH2:7][C:4]3[NH:3][C:2](=[O:1])[NH:6][N:5]=3)(=[O:9])=[O:10])=[CH:13][CH:14]=2)[CH:23]=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 222AmmoniaHCID 887MethanolHCID 1360545044'-({[(5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)methyl]sulfonyl}methyl)biphenyl-3-carbonitrile

생성물 1

HCID 1360544705-[({[3'-(aminomethyl)biphenyl-4-yl]methyl}sulfonyl)methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one수율 99%

시약·촉매·용매 2

HCID 935Nickel촉매
HCID 8028
Tetrahydrofuran
용매

실험 절차

A suspension of 4′-({[(5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)methyl]sulfonyl}methyl)biphenyl-3-carbonitrile obtained in Reference Example 110 (0.250 g, 0.705 mmol), Raney-nickel (0.250 g) and 28% aqueous ammonia (5 mL) in THF (5 mL)-methanol (5 mL) was stirred at room temperature for 4 hr under hydrogen atmosphere (1 atm). The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. Diethyl ether was added to the residue, and the precipitated solid was collected by filtration to give the title compound as a pale-blue powder (0.250 g, 99%).

후처리

  1. filtrationThe insoluble material was filtered off
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. additionDiethyl ether was added to the residue
  4. filtrationthe precipitated solid was collected by filtration

출처 및 근거

ORD 기록
ord-4240a1ad37f94f2c89ec042cc0a05d8a
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915267B2

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