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2-Chlorobenzoyl chloride → (R)-Methyl 3-(2-chloro-N-isobutylbenzamido)-2,3-dihydro-1H-indene-5-carboxylate

HRID 1193272
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HRID 1193272 반응식
[CH2:1]([NH:5][C@H:6]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:15]([O:17][CH3:18])=[O:16])[CH:13]=2)[CH2:8][CH2:7]1)[CH:2]([CH3:4])[CH3:3].[Cl:19][C:20]1[CH:28]=[CH:27][CH:26]=[CH:25][C:21]=1[C:22](Cl)=[O:23]>ClCCl>[Cl:19][C:20]1[CH:28]=[CH:27][CH:26]=[CH:25][C:21]=1[C:22]([N:5]([C@H:6]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:15]([O:17][CH3:18])=[O:16])[CH:13]=2)[CH2:8][CH2:7]1)[CH2:1][CH:2]([CH3:4])[CH3:3])=[O:23]
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참가 물질

4

반응물 2

HCID 691102-Chlorobenzoyl chlorideHCID 66799099(R)-Methyl 3-(isobutylamino)-2,3-dihydro-1H-indene-5-carboxylate

생성물 1

HCID 66799128(R)-Methyl 3-(2-chloro-N-isobutylbenzamido)-2,3-dihydro-1H-indene-5-carboxylate수율 51%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

TEA (1.4 ml, 10.1 mmol, 2.5 eq) was added dropwise at 0° C. to a solution of (R)-methyl 3-(isobutylamino)-2,3-dihydro-1H-indene-5-carboxylate (A-08) (1.0 g, 4.04 mmol, 1 eq) in dichloromethane (25 ml), and stirring was carried out for 15 min. Then 2-chlorobenzoic acid chloride (0.61 ml, 4.858 mmol, 1.2 eq) was added at that temperature, and stirring was carried out for 1 h at RT. After monitoring by thin-layer chromatography, the reaction mixture was diluted with dichloromethane (75 ml), washed with water and sat. NaCl solution (in each case 50 ml), dried over sodium sulfate and purified by column chromatography (silica gel, 2% MeOH in dichloromethane). Yield: 51% (800 mg, 2.078 mmol).

후처리

  1. stirringstirring
  2. waitwas carried out for 1 h at RT
  3. washwashed with water and sat. NaCl solution (in each case 50 ml),
  4. dry with materialdried over sodium sulfate
  5. custompurified by column chromatography (silica gel, 2% MeOH in dichloromethane)

출처 및 근거

ORD 기록
ord-798ced0fcfe64aa1aa334c91fc8d2829
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680159B2

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