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Butyl nitrite → HCID 86586089, 화합물

HRID 1825336
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HRID 1825336 반응식
[C:1]1([NH:7][C@H:8]([C:10]([OH:12])=[O:11])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:13](OCCCC)=[O:14]>COCCOC>[N:13]([N:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[C@H:8]([C:10]([OH:12])=[O:11])[CH3:9])=[O:14]
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참가 물질

4

반응물 2

HCID 10996Butyl nitriteHCID 817923phenyl-Alanine

생성물 1

HCID 86586089HCID 86586089, 화합물

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

N-Phenylalanine (825 mg) in 1,2-dimethoxyethane (20 ml) was treated with n-butyl nitrite (0.64 ml) and the mixture was stirred for 2.5 h and then the solvent was removed to leave crude N-nitroso-N-phenylalanine. This was dissolved in dichloromethane (10 ml), cooled in an ice-bath and treated with trifluoroacetic anhydride (1.06 ml). The mixture was stirred for 1 h and then the solvents were removed, toluene was added and removed using a rotary evaporator. The residue was chromatographed on silica gel eluting with ethanol/chloroform mixtures to give the sydnone (1 g), υmax(CH2Cl2) 1803(sh), 1763(sh), 1734, 1485, 1243, and 1065 cm−1; δ(CDCl3) 2.16 (3H,s), 7.51-7.73 (5H, m); Found m/z 176.0590; C9H8N2O2 requires 176.0586. The sydnone in xylene (8 ml) was treated with ethynyltributylstannane and the mixture was heated under reflux for 8 h. After standing for 16 h at room temperature the mixture was diluted with hexane(15 ml) and loaded onto silica gel and eluted with hexane (100 ml) followed by hexane/ethyl acetate mixtures to give 5-methyl-2-phenyl-3-(tri-n-butylstannyl)pyrazole (602 mg), δ(CDCl3) 0.87-1.76 (27H, m), 2.35 (3H, s), 6.25 (1H, s), 7.26-7.47 (5H, m); Found m/z 448.1900. C22H36N2Sn requires 448.1900.

후처리

  1. customthe solvent was removed

출처 및 근거

ORD 기록
ord-5eb56e9cfbad4dcaadc48a03e0b89b93
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045619B2

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