Triethylamine → 1-{4-[2-(1-Pyrrolyl)benzoylamino]benzoyl}-1,2,3,4tetrahydroquinoline

HRID 441242

反応式

HRID 441242 の反応式
[N:1]1([C:6]2[CH:14]=[CH:13][CH:12]=[CH:11][C:7]=2[C:8]([OH:10])=O)[CH:5]=[CH:4][CH:3]=[CH:2]1.P(Cl)(OC1C=CC=CC=1)(OC1C=CC=CC=1)=O.[NH2:32][C:33]1[CH:50]=[CH:49][C:36]([C:37]([N:39]2[C:48]3[C:43](=[CH:44][CH:45]=[CH:46][CH:47]=3)[CH2:42][CH2:41][CH2:40]2)=[O:38])=[CH:35][CH:34]=1.C(N(CC)CC)C>O1CCCC1>[N:1]1([C:6]2[CH:14]=[CH:13][CH:12]=[CH:11][C:7]=2[C:8]([NH:32][C:33]2[CH:50]=[CH:49][C:36]([C:37]([N:39]3[C:48]4[C:43](=[CH:44][CH:45]=[CH:46][CH:47]=4)[CH2:42][CH2:41][CH2:40]3)=[O:38])=[CH:35][CH:34]=2)=[O:10])[CH:2]=[CH:3][CH:4]=[CH:5]1

参加物

6

反応物 4

HCID 8471TriethylamineHCID 75654Diphenyl chlorophosphateHCID 7285212-(1H-pyrrol-1-yl)benzoic acidHCID 2984117(4-aminophenyl)(3,4-dihydroquinolin-1(2H)-yl)methanone

生成物 1

HCID 105982751-{4-[2-(1-Pyrrolyl)benzoylamino]benzoyl}-1,2,3,4tetrahydroquinoline収率 60.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 2-(1-pyrrolyl)benzoic acid (206 mg), diphenyl chlorophosphate (325 mg), 1-(4-aminobenzoyl}-1,2,3,4-tetrahydroquinoline (277 mg) in tetrahydrofuran (10 ml) was added triethylamine (333 mg) at 0° C. The resulting mixture was allowed to warm to ambient temperature where it was maintained for 5 hours. The solvent was evaporated and diluted with ethyl acetate and washed with water, saturated sodium bicarbonate aqueous solution and brine. The organic layer was dried over sodium sulfate and concentrated to give 1-{4-[2-(1-pyrrolyl)benzoylamino]benzoyl}-1,2,3,4tetrahydroquinoline (280 mg).

後処理

  1. temperaturewas maintained for 5 hours
  2. customThe solvent was evaporated
  3. additiondiluted with ethyl acetate
  4. washwashed with water, saturated sodium bicarbonate aqueous solution and brine
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-b85ecc7cd5d44739bc7c54ad7db59d8c
出典データセット
uspto-grants-1996_05
特許番号
US05521170

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