Triethylamine → (4-Chloropyridin-2-yl)-(5-fluoro-2,3-dihydroindol-1-yl)-methanone

HRID 74509노트

반응식

HRID 74509 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH2:6][CH2:5]2.[Cl:11][C:12]1[CH:17]=[CH:16][N:15]=[C:14]([C:18](O)=[O:19])[CH:13]=1.C(N(CC)CC)C.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F>CN(C=O)C>[Cl:11][C:12]1[CH:17]=[CH:16][N:15]=[C:14]([C:18]([N:7]2[C:8]3[C:4](=[CH:3][C:2]([F:1])=[CH:10][CH:9]=3)[CH2:5][CH2:6]2)=[O:19])[CH:13]=1

참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 2308904-Chloropyridine-2-carboxylic acidHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 27744635-Fluoroindoline

생성물 1

HCID 58386740(4-Chloropyridin-2-yl)-(5-fluoro-2,3-dihydroindol-1-yl)-methanone

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

174 mg (1.27 mmol) 5-fluoro-2,3-dihydro-1H-indole were added to 200.0 mg (1.27 mmol) 4-chloropyridine-2-carboxylic acid, 351 μL (2.50 mmol) triethylamine and 434.0 mg (1.35 mmol) TBTU in 3 mL DMF. The reaction mixture was stirred overnight at RT. Purification was carried out by preparative HPLC. The product fractions were combined and evaporated down i. vac.

후처리

  1. customPurification
  2. customevaporated down i

출처 및 근거

ORD 기록
ord-2734c073f2eb46e681607cbaafcd9340
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08829006B2

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