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Borane;tetrahydrofuran → 2(1H)-Quinolinone, 5-[(1R)-2-chloro-1-hydroxyethyl]-8-(phenylmethoxy)-

HRID 1290066
ノート
印刷プレビュー

反応式

HRID 1290066 の反応式
B.O1CCCC1.CB1N2CCC[C@@H]2C(C2C=CC=CC=2)(C2C=CC=CC=2)O1.[CH2:28]([O:35][C:36]1[CH:37]=[CH:38][C:39]([C:47](=[O:50])[CH2:48][Cl:49])=[C:40]2[C:45]=1[NH:44][C:43](=[O:46])[CH:42]=[CH:41]2)[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>O1CCCC1>[CH2:28]([O:35][C:36]1[CH:37]=[CH:38][C:39]([C@@H:47]([OH:50])[CH2:48][Cl:49])=[C:40]2[C:45]=1[NH:44][C:43](=[O:46])[CH:42]=[CH:41]2)[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 2723981Borane;tetrahydrofuranHCID 9838490(R)-2-Methyl-CBS-oxazaborolidineHCID 109035505-(2-chloroacetyl)-8-phenylmethoxy-1H-quinolin-2-one

生成物 1

HCID 118096612(1H)-Quinolinone, 5-[(1R)-2-chloro-1-hydroxyethyl]-8-(phenylmethoxy)-

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
5 °C

実験手順

Borane-tetrahydrofuran complex (1M in tetrahydrofuran, 1 ml, 1 mMol) was added dropwise to a solution of (R)-tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo [1,2-c][1,3,2]oxazaborole (0.1 equiv, 30 mg, 0.1 mMol) in tetrahydrofuran (6 ml) at ambient temperature under an argon atmosphere. After 5 minutes, 8-benzyloxy-5-chloroacetylcarbostyril (328 mg, 1 mMol) was added and the reaction mixture was stirred for a further 15 minutes. The reaction mixture was cooled to 5° C. and quenched by the dropwise addition of methanol (2 ml). The quenched reaction mixture was stirred for 15 minutes at 5° C. and for 30 minutes at ambient temperature. The solvent was evaporated and the residue was purified by chromatography on silica gel eluting with 10% methanol in ethyl acetate to afford the title compound as a pale yellow solid; m.p. 148°-149° C.; [α]D25 -9.0° (c=1, methanol).

後処理

  1. customquenched by the dropwise addition of methanol (2 ml)
  2. customThe quenched reaction mixture
  3. stirringwas stirred for 15 minutes at 5° C. and for 30 minutes at ambient temperature
  4. customThe solvent was evaporated
  5. customthe residue was purified by chromatography on silica gel eluting with 10% methanol in ethyl acetate

出典と根拠

ORDレコード
ord-16b39d2cbe2a47a1b4de2d047b306c67
出典データセット
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05750701

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート