Triphenylphosphine → 1,4-Dihydrocinnoline

HRID 515519ノート

反応式

HRID 515519 の反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](CO)=[CH:3][N:2]=1.N1C2C(=CC=CC=2)C(CO)C=N1.CN1C2N=C(Cl)N(CC=C(C)C)C=2C(=O)NC1=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>O1CCCC1>[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH:3]=[N:2]1

参加物

7

反応物 5

HCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 220297223-Methyl-7-(3-methyl-2-buten-1-yl)-8-chloro-xanthineHCID 23560691Cinnolin-4-ylmethanolHCID 57514546(1,4-Dihydro-cinnolin-4-yl)methanol

生成物 1

HCID 124272971,4-Dihydrocinnoline

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

510 mg of a mixture of (cinnolin-4-yl)-methanol and (1,4-dihydro-cinnolin-4-yl)-methanol (see Ex. XXVII) are added to 830 mg of 3-methyl-7-(3-methyl-2-buten-1-yl)-8-chloro-xanthine and 1.25 g of triphenylphosphine in 25 ml of tetrahydrofuran. The reaction mixture is combined with 0.92 ml diethyl azodicarboxylate and stirred overnight at ambient temperature. Then it is evaporated down and chromatographed through a silica gel column with ethyl acetate/petroleum ether (7:3 to 0:1) as eluant. A mixture of cinnoline and 1,4-dihydro-cinnoline compound is obtained.

後処理

  1. customThen it is evaporated down
  2. customchromatographed through a silica gel column with ethyl acetate/petroleum ether (7:3 to 0:1) as eluant
  3. additionA mixture of cinnoline

出典と根拠

ORDレコード
ord-bcf2d3dd1cc4428581051e86f73922cc
出典データセット
uspto-grants-2015_08
特許番号
US09108964B2

反応ノート

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