Dicyclopropylmethoxybenzoyl chloride → (+/-)-Acetic acid (1RS,3RS,4RS)-4-{[1-(3,4-bis-cyclopropylmethoxyphenyl)methanoyl]-amino}-3-(3,4-dimethoxyphenyl)cyclohexyl ester

HRID 1867467ノート

反応式

HRID 1867467 の反応式
[NH2:1][CH:2]1[CH2:7][CH2:6][CH:5]([O:8][C:9](=[O:11])[CH3:10])[CH2:4][CH:3]1[C:12]1[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[C:14]([O:20][CH3:21])[CH:13]=1.[CH:22]1([CH2:25][O:26][C:27]2[CH:28]=[C:29]([CH:33]=[CH:34][C:35]=2[O:36][CH2:37][CH:38]2[CH2:40][CH2:39]2)[C:30](Cl)=[O:31])[CH2:24][CH2:23]1.C1(C(C2CC2)OC2C=CC=CC=2C(Cl)=O)CC1>C(Cl)Cl.N1C=CC=CC=1.CN(C)C1C=CN=CC=1>[CH:22]1([CH2:25][O:26][C:27]2[CH:28]=[C:29]([C:30]([NH:1][CH:2]3[CH2:7][CH2:6][CH:5]([O:8][C:9](=[O:11])[CH3:10])[CH2:4][CH:3]3[C:12]3[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[C:14]([O:20][CH3:21])[CH:13]=3)=[O:31])[CH:33]=[CH:34][C:35]=2[O:36][CH2:37][CH:38]2[CH2:39][CH2:40]2)[CH2:24][CH2:23]1

参加物

7

反応物 3

HCID 17989077Dicyclopropylmethoxybenzoyl chlorideHCID 179890793,4-Bis(cyclopropylmethoxy)benzoyl chlorideHCID 67022805acetic acid (1RS,3RS,4RS)-4-amino-3-(3,4-dimethoxyphenyl)cyclohexyl ester2 回

生成物 1

HCID 86601277(+/-)-Acetic acid (1RS,3RS,4RS)-4-{[1-(3,4-bis-cyclopropylmethoxyphenyl)methanoyl]-amino}-3-(3,4-dimethoxyphenyl)cyclohexyl ester

試薬・触媒・溶媒 3

HCID 142844-(Dimethylamino)pyridine触媒2 回HCID 1049Pyridine溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

590 mg of (±)-acetic acid (1RS,3RS,4RS)-4-amino-3-(3,4-dimethoxyphenyl)cyclohexyl ester (compound B1) are dissolved in a mixture of 6 ml of methylene chloride and 1.5 ml of pyridine and 10 mg of 4-dimethylaminopyridine are added. A solution of 595 mg of 3,4-dicyclopropylmethoxybenzoyl chloride in methylene chloride is added dropwise and the mixture is stirred for 16 h. Further 140 mg of dicyclopropylmethoxybenzoyl chloride and 10 mg of 4-dimethylaminopyridine are added to complete the reaction. The solvents are removed and the residue is purified by chromatography on silica gel using a mixture of petroleum ether/ethyl acetate/triethylamine in the ratio 5/4/1 as eluent. After concentration of the corresponding eluate fractions, 630 mg (59% of theory) of the title compound are obtained as a colourless foam.

後処理

  1. additionare added
  2. customthe reaction
  3. customThe solvents are removed
  4. customthe residue is purified by chromatography on silica gel using
  5. additiona mixture of petroleum ether/ethyl acetate/triethylamine in the ratio 5/4/1 as eluent

出典と根拠

ORDレコード
ord-1ec1c8f310624d0d8cb8bccd072f1dc8
出典データセット
uspto-grants-2009_12
特許番号
US07632844B2

反応ノート

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