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Pyridine → HCID 178485750、化合物

HRID 1031754
ノート
印刷プレビュー

反応式

HRID 1031754 の反応式
Cl.CN(C)C(=O)[C@H]([CH2:7][C:8]1[CH:13]=CC=C[CH:9]=1)N.Cl.N(C1C=CC([C:25]([OH:27])=[O:26])=CC=1)C(N)=N.[CH:30]1([N:36]=C=NC2CCCCC2)CCCCC1.N([C:49]1[CH:68]=[CH:67][C:52]([C:53]([NH:55][C@H:56]([C:64]([OH:66])=O)[CH2:57][C:58]2[CH:63]=[CH:62][CH:61]=[CH:60][CH:59]=2)=[O:54])=[CH:51][CH:50]=1)C(N)=N.[N:69]1C=CC=C[CH:70]=1>>[CH3:30][NH:36][C:64](=[O:66])[C@H:56]([CH2:57][C:58]1[CH:59]=[CH:60][CH:61]=[CH:62][CH:63]=1)[NH:55][C:53]([C@H:52]1[CH2:51][CH2:50][C@H:49]([CH2:70][NH:69][C:25]([O:27][C:8]([CH3:7])([CH3:9])[CH3:13])=[O:26])[CH2:68][CH2:67]1)=[O:54]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 1049PyridineHCID 10868DicyclohexylcarbodiimideHCID 12653778(2S)-2-Amino-N,N-dimethyl-3-phenylpropanamide hydrochloride2 回HCID 178479383HCID 178479383、化合物HCID 178512528HCID 178512528、化合物

生成物 1

HCID 178485750HCID 178485750、化合物

実験手順

After evaporation of the solvent, the residue was extracted with ethyl acetate, washed with water, and dried over sodium sulfate. After evaporation of the solvent, a white powder of N-(t-butoxycarbonyl)-L-phenylalanine 4-cis/trans-methylcyclohexylamide (I) (0.5 g) was obtained. After confirmation by NMR and IR, 4N hydrogen chloride/1,4-dioxane solution (5 ml) was added to the above compound (I) (0.5 g) under ice-cooling, and the mixture was stirred at room temperature for 30 minutes. Hexane (20 ml) was added and the solids precipitated were washed several times with diethyl ether to obtain white solids (0.45 g) of L-phenylalanine 4-cis/trans-methylcyclohexylamide hydrochloride (II). This structure was confirmed by NMR spectrum. To the mixture of 4-guanidino benzoic acid hydrochloride, dry pyridine (3 ml) and 1,3-dicyclohexylcarbodiimide (0.36 g), the above compound (II) was added under ice-cooling, and the mixture was left to stand at room temperature for 12 hours. After a conventional post-treatment, pale yellow solids of N-(4-guanidinobenzoyl)-L-phenylalanine 4-cis/trans-methylcyclohexylamide (III) (0.5 g) were obtained. After confirmation by NMR, the above compound (III) (0.5 g) was added to a saturated sodium hydrogen carbonate solution (10 ml) and the mixture was stirred for 5 minutes, followed by a recovery of the precipitates. After washing several times with water, pale yellow solids of N-(4-guanidinobenzoyl)-L-phenylalanine 4-cis/trans-methylcyclohexylamide carbonate (IV) (0.25 g). After confirmation by IR, the above compound (IV) (0.2 g) was added to a 4N hydrogen chloride/1,4-dioxane solution (1 ml) under ice-cooling, and the mixture was stirred for 20 minutes. Diethyl ether was then added, and the precipitated solids were washed several times with diethyl ether to obtain N-(4-guanidinobenzoyl)-L-phenylalanine 4-cis/transmethylcyclohexylamide hydrochloride (0.15 g) as pale yellow solids.

後処理

  1. temperaturecooling
  2. waitthe mixture was left

出典と根拠

ORDレコード
ord-fd5ce8bf0eb8481c98063a7ab0636093
出典データセット
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04954512

反応ノート

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