Ammonia → 2-[1-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-6,8-dimethoxy-isoquinolin-4-ylamino]-thiazole-4-carboxylic acid

HRID 14694

반응식

HRID 14694 반응식
[C:1](Cl)(Cl)=[S:2].[NH2:5][C:6]1[C:15]2[C:10](=[C:11]([O:18][CH3:19])[CH:12]=[C:13]([O:16][CH3:17])[CH:14]=2)[C:9]([CH2:20][N:21]2[C:29](=[O:30])[C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[C:22]2=[O:31])=[N:8][CH:7]=1.C[CH2:33][N:34](C(C)C)C(C)C.N.BrC[C:44](=O)[C:45]([OH:47])=[O:46]>C1COCC1>[O:31]=[C:22]1[C:23]2[C:28](=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:29](=[O:30])[N:21]1[CH2:20][C:9]1[C:10]2[C:15](=[CH:14][C:13]([O:16][CH3:17])=[CH:12][C:11]=2[O:18][CH3:19])[C:6]([NH:5][C:33]2[S:2][CH:1]=[C:44]([C:45]([OH:47])=[O:46])[N:34]=2)=[CH:7][N:8]=1

참가 물질

7

실험 절차

Thiophosgene (146 μL, 1.92 mmol) was added to a solution of Example 45C (580 mg, 1.6 mmol) and DIEA (670 μL) in THF (10 mL). After stirring for 1 h, the reaction was poured over aqueous ammonia and extracted with EtOAc. Organics were dried (MgSO4) and concentrated. The resulting crude thiourea was dissolved in THF (5 mL). Bromopyruvic acid (320 mg, 1.92 mmol) was added, and the reaction stirred for 2 h. Purification by silica gel chromatography (10% MeOH/CHCl3) gave 590 mg (75%) of the title compound as a tan solid. H1-NMR (MeOD-d4): δ 9.95 (br s, 1H), 8.81 (br s, 1H), 7.87-7.96 (m, 4H), 7.60 (br s, 1H), 7.14 (s, 1H), 6.86 (s, 1H), 5.41 (s, 2H), 4.09 (s, 3H), 3.94 (s, 3H). MS (ES) (M+H) calc'd for C24H18N4O6S, 491; found 491.

후처리

  1. extractionextracted with EtOAc
  2. dry with materialOrganics were dried (MgSO4)
  3. concentrationconcentrated
  4. dissolutionThe resulting crude thiourea was dissolved in THF (5 mL)
  5. stirringthe reaction stirred for 2 h
  6. customPurification by silica gel chromatography (10% MeOH/CHCl3)

출처 및 근거

ORD 기록
ord-aac9a72a39a84e959ebd805c61d91840
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07732446B1

연결된 노트

불러오는 중…