Lithium Hydroxide → 3-{N-[1(S)-(3,4-dichlorophenyl)ethyl]amino}-2(S)-hydroxy-propyl-(cyclohex-3-enylmethyl)-phosphinic acid

HRID 1440685ノート

反応式

HRID 1440685 の反応式
[OH-].[Li+].C([O:5][P:6]([CH2:15][C@@H:16]([OH:18])[CH3:17])([CH2:8][CH:9]1[CH2:14][CH2:13][CH:12]=[CH:11][CH2:10]1)=[O:7])C.BrCC1CCC=CC1.C(OP(C(OCC)(OCC)C)=O)C.C(OP(C[C@@H](O)CCl)(CC1CCC=CC1)=O)C.[Cl:57][C:58]1[CH:59]=[C:60]([C@@H:65]([NH2:67])[CH3:66])[CH:61]=[CH:62][C:63]=1[Cl:64]>O.C(O)C>[Cl:57][C:58]1[CH:59]=[C:60]([C@@H:65]([NH:67][CH2:17][C@H:16]([OH:18])[CH2:15][P:6]([CH2:8][CH:9]2[CH2:14][CH2:13][CH:12]=[CH:11][CH2:10]2)(=[O:7])[OH:5])[CH3:66])[CH:61]=[CH:62][C:63]=1[Cl:64]

参加物

9

反応物 6

HCID 3939Lithium HydroxideHCID 5654734-(Bromomethyl)cyclohexeneHCID 793512(S)-1-(3,4-Dichlorophenyl)ethanamineHCID 541698053-chloro-2(R)-hydroxy-propyl-(cyclohex-3-enylmethyl)phosphinic acid ethyl esterHCID 867483482(S)-hydroxy-propyl-(cyclohex-3-enylmethyl)-phosphinic acid ethyl esterHCID 178476820HCID 178476820、化合物

生成物 1

HCID 599034363-{N-[1(S)-(3,4-dichlorophenyl)ethyl]amino}-2(S)-hydroxy-propyl-(cyclohex-3-enylmethyl)-phosphinic acid

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A solution of 0.13 g of lithium hydroxide in 3 ml of water is added to a solution in 5 ml of ethanol of 1.1 g of 3-{N-1(S)-(3,4-dichlorophenyl)ethyl]amino}-2(S)-hydroxy-propyl-(cyclohex-3-enylmethyl)-phosphinic acid ethyl ester [obtainable as described in Example 2 starting from bromomethylcyclohex-3-ene and 1,1-diethoxyethylphosphinic acid ethyl ester via 3-chloro-2(R)-hydroxy-propyl-(cyclohex-3-enylmethyl)phosphinic acid ethyl ester and further reaction thereof with 1(S)-(3,4-dichlorophenyl)ethylamine] and the mixture is heated at 60° for 24 hours, then cooled to room temperature and concentrated by evaporation under reduced pressure. The residue is taken up in water, rendered neutral with aqueous phosphoric acid solution and again concentrated by evaporation under reduced pressure. The white solid that remains behind is taken up in hot methanol and filtered. Removal of the methanol yields a hygroscopic solid which, after crystallisation from cyclohexane/petroleum ether (60°-80°), yields 3-{N-[1(S)-(3,4-dichlorophenyl)ethyl]amino}-2(S)-hydroxy-propyl-(cyclohex-3-enylmethyl)-phosphinic acid in the form of a hygroscopic solid; 1H-NMR spectrum (in CD3OD): δ=7.68 (1H), 7.58 (1H), 7.40 (1H), 6.60 (2H, CH=CH), 4.22 (1H, q, CH), 4.13 (1H, m), 2.97 (1H, dd), CHN), 2.63 (1H, dd, CHN), 2.33-1.21 (14H, m). The hydrochloride melts at 105°-206°.

後処理

  1. concentrationconcentrated by evaporation under reduced pressure
  2. concentrationagain concentrated by evaporation under reduced pressure
  3. filtrationfiltered
  4. customRemoval of the methanol
  5. customyields a hygroscopic solid which
  6. customafter crystallisation from cyclohexane/petroleum ether (60°-80°)

出典と根拠

ORDレコード
ord-00dde838d7aa4bf0b5a9f26674d7de52
出典データセット
uspto-grants-1996_03
特許番号
US05500418

反応ノート

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