1,2-Dichloroethane → 3-(3,4-Difluorophenyl)-3-methoxypyrrolidine

HRID 575953ノート

反応式

HRID 575953 の反応式
C([N:8]1[CH2:12][CH2:11][C:10]([C:15]2[CH:20]=[CH:19][C:18]([F:21])=[C:17]([F:22])[CH:16]=2)([O:13][CH3:14])[CH2:9]1)C1C=CC=CC=1.ClCCCl.ClC(OC(Cl)C)=O>CO>[F:22][C:17]1[CH:16]=[C:15]([C:10]2([O:13][CH3:14])[CH2:11][CH2:12][NH:8][CH2:9]2)[CH:20]=[CH:19][C:18]=1[F:21]

参加物

5

反応物 3

HCID 111,2-DichloroethaneHCID 5213051-Chloroethyl chloroformateHCID 674032321-Benzyl-3-(3,4-difluorophenyl)-3-methoxypyrrolidine

生成物 1

HCID 462192213-(3,4-Difluorophenyl)-3-methoxypyrrolidine収率 97.6%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Preparation according to Example 1. (−)-1-benzyl-3-(3,4-difluorophenyl)-3-methoxypyrrolidine (0.264 g, 0.87 mmol), 1,2-dichloroethane (20 ml), 1-chloroethyl chloroformate (0.49 g, 3.48 mmol) refluxed for 1 h, and methanol (20 ml) reflux 1 h Purification by HPLC on waters OBD C18, 5 μm (MeOH/33 mM NH3, 20:80 to 50:50) gave the title compound (0.181 g, 97%). [a]D=−6.1° (methanol). MS m/z (rel. intensity, 70 eV) 213 (M+, 1), 198 (51), 183 (88), 171 (bp), 141 (53).

後処理

  1. customPreparation
  2. customPurification by HPLC on waters OBD C18, 5 μm (MeOH/33 mM NH3, 20:80 to 50:50)

出典と根拠

ORDレコード
ord-758722f5b9c14e50b128b0aecd65d1cb
出典データセット
uspto-grants-2015_05
特許番号
US09035073B2

反応ノート

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