Triethylamine → 6-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-indole-1-carboxylic acid tert-butyl ester
반응식
[F:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)=[C:4]([O:16][CH3:17])[CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O.[C:51]([O:55][C:56]([N:58]1[C:66]2[C:61](=[CH:62][CH:63]=[C:64]([CH2:67]O)[CH:65]=2)[CH:60]=[CH:59]1)=[O:57])([CH3:54])([CH3:53])[CH3:52].C(N(CC)CC)C>ClCCl>[C:51]([O:55][C:56]([N:58]1[C:66]2[C:61](=[CH:62][CH:63]=[C:64]([CH2:67][O:15][C:12]3[CH:11]=[CH:10][C:9]([C:5]4[CH:6]=[C:7]([F:8])[C:2]([F:1])=[CH:3][C:4]=4[O:16][CH3:17])=[CH:14][CH:13]=3)[CH:65]=2)[CH:60]=[CH:59]1)=[O:57])([CH3:54])([CH3:53])[CH3:52]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
To 4′,5′-difluoro-2′-methoxy-biphenyl-4-ol (472 mg, 2 mmol, 2 eq) was added polymer-bound triphenyl-phosphine (667 mg, 2 mmol, 2 eq) and dichloromethane (10 mL). The mixture was placed under nitrogen, cooled in an ice bath, diisopropyl azodicarboxylate (0.394 mL, 2 mmol, 2 eq) was added drop-wise, stirred for 1.5 hr. A solution of 6-hydroxymethyl-indole-1-carboxylic acid tert-butyl ester (247 mg, 1 mmol, 1 eq) and triethylamine (0.279 mL, 2 mmol, 2 eq) in dichloromethane (2 mL) was added drop to portion wise and the reaction allowed to warm to room temperature overnight (20 hr). The reaction was filtered over Celite, adsorbed onto silica gel, and purified by flash chromatography with a gradient from 1-15% ethyl acetate in hexanes to yield 6-(4′,5′-difluoro-2′-methoxy-biphenyl-4-yloxymethyl)-indole-1-carboxylic acid tert-butyl ester white/clear solid (288 mg, 62%). LC-MS (ES) calculated for C27H25F2NO2, 465.2; found m/z 466 [M+H]+.
후처리
- temperaturecooled in an ice bath
- filtrationThe reaction was filtered over Celite
- custompurified by flash chromatography with a gradient from 1-15% ethyl acetate in hexanes
출처 및 근거
- ORD 기록
- ord-cf1e06e22be74a118288876d3ebb2712
- 출처 데이터셋
- uspto-grants-2011_05
- 특허 번호
- US07947728B1
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