4-Methylmorpholine → (R)-3-mercapto-2-[(S)-2-methyl-3-trityloxy-propionylamino]-propionic acid methyl ester

HRID 234211

反応式

HRID 234211 の反応式
[C:1]([O:20][C@@H](C)C(O)=O)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[CH3:27][O:28][C:29](=[O:34])[C@H:30]([CH2:32][SH:33])[NH2:31].Cl.CN(C)[CH2:38][CH2:39][CH2:40]N=C=NCC.CN1CC[O:51][CH2:50]C1>C(#N)C>[CH3:27][O:28][C:29](=[O:34])[C@@H:30]([NH:31][C:50](=[O:51])[C@@H:39]([CH3:38])[CH2:40][O:20][C:1]([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)[CH2:32][SH:33]

参加物

6

反応物 4

HCID 79724-MethylmorpholineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2733208L-Cysteine, methyl ester, hydrochlorideHCID 54161083(S)-2-trityloxypropionic acid

生成物 1

HCID 54008528(R)-3-mercapto-2-[(S)-2-methyl-3-trityloxy-propionylamino]-propionic acid methyl ester収率 16.5%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒2 回

実験手順

To a suspension of 9.97 g of (S)-2-trityloxy-propionic acid, 5.60 g of L-cysteine methyl ester hydrochloride and 6.6 g of N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride in 50 ml acetonitrile was added over 10 min a solution of 6.9 g of 4-methyl-morpholine in 50 ml of acetonitrile. The mixture was stirred at room temperature for 3 h and then partitioned between water and ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel using ethyl acetate/hexane (1:2, v/v) as eluent to yield 2.30 g of (R)-3-mercapto-2-[(S)-2-methyl-3-trityloxy-propionylamino]-propionic acid methyl ester as amorphous solid. 1H-NMR (250 MHz,DMSO-d6): δ0.88(d,J=10 Hz,3H); 2.42(t,J=15 Hz, 1H); 2.78 (dd,J=10 Hz and 15 Hz,2H); 3.66(s,3H); 4.01(q,J=10 Hz, 1H); 4.20-4.30(m, 1H); 7.25-7.50(m, 16H); 7.82(d,J=16 Hz,1H) ppm.

後処理

  1. custompartitioned between water and ethyl acetate
  2. washThe organic layer was washed with brine
  3. dry with materialdried over magnesium sulfate
  4. customevaporated in vacuo
  5. customThe residue was chromatographed on silica gel

出典と根拠

ORDレコード
ord-e0c84cc91f1d439183e58be7b2c7be11
出典データセット
uspto-grants-1997_01
特許番号
US05594135

関連ノート

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