Hippuric Acid → 3-(N-benzoylglycyl)amino-1-(4-chlorobenzyl)pyrrolidine

HRID 2187763

반응식

HRID 2187763 반응식
[C:1]([NH:9][CH2:10][C:11]([OH:13])=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.ON1C2C=CC=CC=2N=N1.Cl.Cl.[NH2:27][CH:28]1[CH2:32][CH2:31][N:30]([CH2:33][C:34]2[CH:39]=[CH:38][C:37]([Cl:40])=[CH:36][CH:35]=2)[CH2:29]1.CCN(CC)CC>C(Cl)(Cl)Cl>[C:1]([NH:9][CH2:10][C:11]([NH:27][CH:28]1[CH2:32][CH2:31][N:30]([CH2:33][C:34]2[CH:39]=[CH:38][C:37]([Cl:40])=[CH:36][CH:35]=2)[CH2:29]1)=[O:13])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

6

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온도
25 °C

실험 절차

N-Benzoylglycine (9.9 mg, 0.055 mmol), 3-ethyl-1-{3(dimethylaminopropyl}carbodiimide hydrochloride (EDCI) (10.5 mg) and 1-hydroxybenzotriazole hydrate (HOBt) (7.4 mg) were added to a solution of 3-amino-1-(4-chlorobenzyl)pyrrolidine dihydrochloride (14.2 mg, 0.050 mmol) and Et3N (15.2 mg) in CHCl3 (2.5 mL). The reaction mixture was stirred at 25° C. for 16 h, washed with 2 N aqueous NaOH (2 mL×2) and brine (1 mL). After filtration through a PTFE membrane filter, the solvent was removed under reduced pressure to afford 3-(N-benzoylglycyl)amino-1-(4-chlorobenzyl)pyrrolidine (compound No. 1) as a pale yellow oil (17.7 mg, 95%): The purity was determined by RPLC/MS (95%); ESI/MS m/e 372.0 (M++H, C20H22ClN3O2).

후처리

  1. washwashed with 2 N aqueous NaOH (2 mL×2) and brine (1 mL)
  2. filtrationAfter filtration through a PTFE membrane
  3. filtrationfilter
  4. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-3412ddd2e14e4ecebbdd9245a447095d
출처 데이터셋
uspto-grants-2002_06
특허 번호
US06410566B1

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