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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Piperidine → Imidazolyl indolinone

HRID 413727
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인쇄 미리보기

반응식

HRID 413727 반응식
C([C:3]1[NH:4][CH:5]=[C:6](C=O)[N:7]=1)C.C1C=CC(C(Cl)(C2C(Cl)=CC=CC=2)C2C=CC=CC=2)=CC=1.N1CCCCC1.[NH:37]1[C:45]2[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=2)[CH2:39][C:38]1=[O:46]>CN(C=O)C>[NH:4]1[CH:5]=[CH:6][N:7]=[C:3]1[N:37]1[C:45]2[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=2)[CH2:39][C:38]1=[O:46]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8082PiperidineHCID 945242-Chlorotrityl chlorideHCID 321710OxindoleHCID 178437699HCID 178437699, 화합물

생성물 1

HCID 23177814Imidazolyl indolinone

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 2-ethyl-4-formylimidazole attached to 2-chlorotrityl resin (4, 78 mg, 0.052 mmol based on 0.67 mmol/g loading), DMF (0.9 ml) and piperidine (0.1 ml) was gently stirred for 45 min. at ambient temperature, afterwhich was added 2-indolinone (5, 70 mg, 0.523 mmol). The resultant mixture was gently stirred and heated at 80° C. for 20 h. The resin was filtered and washed with 30 ml each of acetone, water, dichloromethane, methanol, and another portion of acetone. Finally, the resin was air dried for 20 min.

후처리

  1. temperatureheated at 80° C. for 20 h
  2. filtrationThe resin was filtered
  3. washwashed with 30 ml each of acetone, water, dichloromethane, methanol
  4. customdried for 20 min.

출처 및 근거

ORD 기록
ord-cf0e67eac901434eaae9842178cdff62
출처 데이터셋
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06569868B2

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