반응 #557945

ord-b97d2b40906a4292ae3fa3385ecc61d8

반응 방정식

O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid
Cc1c(F)ccc(C#N)c1Cl
2-chloro-4-fluoro-3-methylbenzonitrile
N[C@H](CO)C(=O)O
H-D-Ser-OH
O=C([O-])[O-].[K+].[K+]
K2CO3
Cc1c(N[C@H](CO)C(=O)O)ccc(C#N)c1Cl
final product
수율 29.3%
Cc1c(N[C@H](CO)C(=O)O)ccc(C#N)c1Cl
(R)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxypropanoic acid
수율 29.3%

용매

반응 조건

온도
75°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was cooled to room temperature
  2. 2
    workup.STIRRINGstirred for 10 min at room temperature
  3. 3
    추출The solution was extracted with EtOAc several times
  4. 4
    기타to get the crude product
  5. 5
    기타The crude product was chromatographed with a gradient of hexanes/EtOAc

실험 절차

2-chloro-4-fluoro-3-methylbenzonitrile (500 mg, 2.95 mmol) was mixed together with H-D-Ser-OH (682 mg, 6.49 mmol) in DMSO (20 mL). K2CO3 (856 mg, 6.19 mmol) was added to the reaction mixture and stirred at 75° C. for 24 h. The reaction mixture was cooled to room temperature and poured slowly in to a 10% citric acid solution and stirred for 10 min at room temperature. The solution was extracted with EtOAc several times to get the crude product. The crude product was chromatographed with a gradient of hexanes/EtOAc and then with EtOAc, 100% to give the final product (220 mg): 1H NMR (500 MHz, DMSO-d6, δ in ppm) 7.47 (d, J=9 Hz, 1H), 6.57 (d, J=9 Hz, 1H), 6.13 (br s, 1H), 3.62 (m, 2H), 2.18 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08629167B2uspto-grants-2014_01