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

tert-butyl 7-chloro-3-iodo-1H-pyrrolo[2,3-c]pyridine-1-carboxylate → tert-butyl 3-(2-tert-butoxy-2-oxoethyl)-7-chloro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate

HRID 513205
노트
인쇄 미리보기

반응식

HRID 513205 반응식
[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[C:10](I)=[CH:9][N:8]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[C:7]=12.[C:19]([O:23][C:24](=[O:28])[CH2:25][Zn]Cl)([CH3:22])([CH3:21])[CH3:20]>C1COCC1.[Pd].C(P)(C)(C)C.C(P)(C)(C)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[C:19]([O:23][C:24](=[O:28])[CH2:25][C:10]1[C:6]2[C:7](=[C:2]([Cl:1])[N:3]=[CH:4][CH:5]=2)[N:8]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH:9]=1)([CH3:22])([CH3:21])[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 86720575tert-butyl 7-chloro-3-iodo-1H-pyrrolo[2,3-c]pyridine-1-carboxylateHCID 178451184HCID 178451184, 화합물

생성물 1

HCID 86720576tert-butyl 3-(2-tert-butoxy-2-oxoethyl)-7-chloro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate수율 80.1%

시약·촉매·용매 3

HCID 167845palladium(II) acetate촉매HCID 57475661
Bis[(1,1-dimethylethyl)phosphanyl]palladium
촉매
HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of tert-butyl 7-chloro-3-iodo-1H-pyrrolo[2,3-c]pyridine-1-carboxylate (500 mg, 1.3 mmol), bis-(tert-butyl-phosphine) palladium (67.5 mg, 0.13 mmol), and palladium acetate (7.4 mg, 0.003 mmol) in THF (10 mL) was added (2-tert-butoxy-2-oxoethyl)(chloro)zinc (6.6 mL, 3.3 mmol, 0.5 M in diethyl ether). The mixture was then heated to 50 C overnight, cooled to r.t. and quenched by addition of MeOH (1 mL). EtOAc was added and the solution was extracted with 5% KHSO4. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The crude material was purified on silica (gradient elution, 0-25% EtOAc/hexanes) to yield the title product (382 mg). HRMS (ESI) calc (M+H)+=367.1419. found 367.1422.

후처리

  1. temperatureThe mixture was then heated to 50 C overnight
  2. customquenched by addition of MeOH (1 mL)
  3. additionEtOAc was added
  4. extractionthe solution was extracted with 5% KHSO4
  5. dry with materialThe organic layer was dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude material was purified on silica (gradient elution, 0-25% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-789126c2baf14fc2a55f482d2db51a46
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102673B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트