Sodium hydride → ({2-[Hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-benzenesulfonyl}-o-tolyl-amino)-acetic acid methyl ester

HRID 1265332

반응식

HRID 1265332 반응식
[H-].[Na+].[OH:3][CH:4]([C:22]1[CH:30]=[C:29]([O:31][CH3:32])[C:25]2[O:26][CH2:27][O:28][C:24]=2[CH:23]=1)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[S:11]([NH:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:21])(=[O:13])=[O:12].Br[CH2:34][C:35]([O:37][CH3:38])=[O:36]>O1CCCC1>[CH3:38][O:37][C:35](=[O:36])[CH2:34][N:14]([S:11]([C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=1[CH:4]([OH:3])[C:22]1[CH:30]=[C:29]([O:31][CH3:32])[C:25]2[O:26][CH2:27][O:28][C:24]=2[CH:23]=1)(=[O:12])=[O:13])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:21]

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 60984Methyl bromoacetateHCID 186155802-[Hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-N-o-tolyl-benzenesulfonamide

생성물 1

HCID 22965597({2-[Hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-benzenesulfonyl}-o-tolyl-amino)-acetic acid methyl ester수율 89.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Sixty percent sodium hydride suspension in oil (0.422 g, 10.55 mmol) was washed with tetrahydrofuran and was added to tetrahydrofuran (175 mL). To this was added 2-[hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-N-o-tolyl-benzenesulfonamide (4.1 g, 9.59 mmol). After stirring for 30 minutes, methyl bromoacetate (1.09 mL, 11.5 mmol) was added followed by stirring at reflux for 18 hours. The mixture was evaporated to an oil in vacuo, and the residue was resuspended in ethyl ether, washed with 1N citric and brine. The solution was dried over anhydrous magnesium sulfate, filtered, and evaporated to a solid. The material was chromatographed on 300 g silica gel eluted with a mixture of ethyl acetate and hexane (35:65). The appropriate fractions were concentrated in vacuo from ethyl ether giving a solid, 4.29 g, 89.5% yield. NMR spectra and elemental analysis were consistent with the structure.

후처리

  1. stirringby stirring
  2. temperatureat reflux for 18 hours
  3. customThe mixture was evaporated to an oil in vacuo
  4. washwashed with 1N citric
  5. dry with materialThe solution was dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customevaporated to a solid
  8. customThe material was chromatographed on 300 g silica gel
  9. washeluted with a mixture of ethyl acetate and hexane (35:65)
  10. concentrationThe appropriate fractions were concentrated in vacuo from ethyl ether giving a solid, 4.29 g, 89.5% yield

출처 및 근거

ORD 기록
ord-d4ae79b639364b7c95cf8c3f88f6d52e
출처 데이터셋
uspto-grants-2003_04
특허 번호
US06545150B2

연결된 노트

불러오는 중…