Diisopropylethylamine → Ethyl (R) 3-{4-[2-(4-methoxy-2-o-tolylaminobenzoxazol-6-yl)acetylamino]phenyl}butanoate

HRID 1357860노트

반응식

HRID 1357860 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([CH3:15])[CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][CH:3]=1.C(N(C(C)C)CC)(C)C.[CH3:25][O:26][C:27]1[C:32]2[N:33]=[C:34]([NH:36][C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=3[CH3:43])[O:35][C:31]=2[CH:30]=[C:29]([CH2:44][C:45](O)=[O:46])[CH:28]=1.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1>CN(C)C=O>[CH3:25][O:26][C:27]1[C:32]2[N:33]=[C:34]([NH:36][C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=3[CH3:43])[O:35][C:31]=2[CH:30]=[C:29]([CH2:44][C:45]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([C@H:8]([CH3:15])[CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:6][CH:7]=2)=[O:46])[CH:28]=1

참가 물질

6

실험 절차

A stirred solution of with ethyl (R) 3-(4-aminophenyl)butanoate (0.107 g, Reference Example 1) in dimethylformamide (10 mL) was treated with diisopropylethylamine (0.4 g), 2-(4-methoxy-2-o-tolylaminobenzoxazol-6-yl)acetic acid [0.105 g, Reference Example 9(a)] and then with O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (0.14 g). The mixture was left to stand for 20 hours and then partitioned between ethyl acetate and hydrochloric acid (1M). The organic phase was washed with water, then with aqueous bicarbonate solution (5%), then with water, then with brine, then dried and then evaporated to give the title compound (0.17 g) as a cream coloured solid.

후처리

  1. waitThe mixture was left
  2. custompartitioned between ethyl acetate and hydrochloric acid (1M)
  3. washThe organic phase was washed with water
  4. dry with materialwith aqueous bicarbonate solution (5%), then with water, then with brine, then dried
  5. customevaporated

출처 및 근거

ORD 기록
ord-c59a1605500a4370b225f4b99379efa6
출처 데이터셋
uspto-grants-2003_07
특허 번호
US06593354B2

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