Dicyclohexylcarbodiimide → 2H-1,4-Benzodiazepin-2-one, 1,3-dihydro-7-chloro-5-phenyl-3-(phenylmethyl)-, (R)-

HRID 620563노트

반응식

HRID 620563 반응식
[NH2:1][C:2]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=O.C([NH:24][C@@H:25]([C:33](O)=[O:34])[CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)(OC(C)(C)C)=O.C1CCC(N=C=NC2CCCCC2)CC1>C(Cl)Cl>[Cl:16][C:13]1[CH:14]=[CH:15][C:2]2[NH:1][C:33](=[O:34])[C@@H:25]([CH2:26][C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[N:24]=[C:4]([C:6]3[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=3)[C:3]=2[CH:12]=1

참가 물질

5

실험 절차

The procedure of Example 1 was carried out using 2-amino-5-chlorobenzophenone (2.32 gm, 0.01 mol), Boc-D-Phenylalanine (2.65 gm, 0.01 mol), and DCC (10 ml of 1.0 M solution in CH2Cl2) in CH2Cl2 (10 ml). After filtration and evaporation, the crude solid was deprotected and cyclized by the procedure of Example 2. After stirring 5 days, the mixture was evaporated in vacuo, treated with H2O (50 ml), and extracted with EtoAc (2×100 ml). The combined organic extracts were washed with brine (50 ml), dried over MgSO4, filtered and evaporated to dryness in vacuo. Chromatogaphy on silica gel eluted with 7.5% (v/v) Et2O in CH2Cl2 gave a white foam which was crystallized from Et2O. The solid was dried in vacuo at 65° C.: (m.p. 154°-7° C.).

후처리

  1. filtrationAfter filtration and evaporation
  2. customthe mixture was evaporated in vacuo
  3. additiontreated with H2O (50 ml)
  4. extractionextracted with EtoAc (2×100 ml)
  5. washThe combined organic extracts were washed with brine (50 ml)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated to dryness in vacuo
  9. washChromatogaphy on silica gel eluted with 7.5% (v/v) Et2O in CH2Cl2
  10. customgave a white foam which
  11. customwas crystallized from Et2O
  12. customThe solid was dried in vacuo at 65° C.

출처 및 근거

ORD 기록
ord-d6d59af268fb4425a626e247665e6807
출처 데이터셋
uspto-grants-1989_04
특허 번호
US04820834

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