홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Potassium bis(trimethylsilyl)amide → ethyl 4-methylene-7,8-dihydro-4H-thieno[2,3-d]azepine-6(5H)-carboxylate

HRID 1365611
노트
인쇄 미리보기

반응식

HRID 1365611 반응식
[CH3:1][Si]([N-][Si](C)(C)C)(C)C.[K+].[CH2:11]([O:13][C:14]([N:16]1[CH2:22][C:21](=O)[C:20]2[CH:24]=[CH:25][S:26][C:19]=2[CH2:18][CH2:17]1)=[O:15])[CH3:12]>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1COCC1>[CH2:11]([O:13][C:14]([N:16]1[CH2:22][C:21](=[CH2:1])[C:20]2[CH:24]=[CH:25][S:26][C:19]=2[CH2:18][CH2:17]1)=[O:15])[CH3:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 3251421Potassium bis(trimethylsilyl)amideHCID 574239834-Oxo-4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester

생성물 1

HCID 58293774ethyl 4-methylene-7,8-dihydro-4H-thieno[2,3-d]azepine-6(5H)-carboxylate수율 87.6%

시약·촉매·용매 2

HCID 74505Methyltriphenyliphosphonium bromide촉매HCID 8028Tetrahydrofuran
용매
2회

반응 조건

온도
0 °C

실험 절차

Methyl triphenylphosphonium bromide (6.3 g, 17.6 mmol) was dissolved in 150 mL THF and cooled to 0° C. KHMDS (3.2 g, 16.2 mmol) was added portionwise and the reaction was stirred for ½ hour. The product of Example 1, step (c) (3.0 g, 12.5 mmol) was added as a solution in 25 μL THF. The reaction was warmed to room temperature and stirred for 1 hour. The mixture was concentrated and the title product was purified by silica gel chromatography (0% to 40% EtOAc in hexanes) to give 2.6 g of the sub-title compound.

후처리

  1. temperatureThe reaction was warmed to room temperature
  2. stirringstirred for 1 hour
  3. concentrationThe mixture was concentrated
  4. customthe title product was purified by silica gel chromatography (0% to 40% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-732b2b189f3848a0a4f877c66026f5e7
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07893051B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트