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

2-Chloropyrimidine-4-carbonitrile → HCID 21959645, 화합물

HRID 1924115
노트
인쇄 미리보기

반응식

HRID 1924115 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8]#[N:9])[CH:5]=[CH:4][N:3]=1.[C:10](OC([O-])=O)([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11]>CO.[Ni]>[C:13]([O:12][C:10](=[O:11])[NH:9][CH2:8][C:6]1[CH:5]=[CH:4][N:3]=[C:2]([Cl:1])[N:7]=1)([CH3:16])([CH3:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2466472-Chloropyrimidine-4-carbonitrileHCID 22064466Tert-butyldicarbonate

생성물 1

HCID 21959645HCID 21959645, 화합물수율 84%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

2-Chloropyrimidine-4-carbonitrile (24 g), 40.8 g of t-butyl dicarbonate (Boc2O) in 1.2 L of methanol and 5 g of Raney nickel (Raney 2400) were charged in an autoclave. The autoclave was sealed and purged with hydrogen. The hydrogenation was run at 30 psi hydrogen gas. The reduction was carried out to completion and the reactor was vented and purged with nitrogen. The reaction mixture was filtered over diatomaceous earth and the filtrate was concentrated. The residue was purified by chromatography to yield the title compound (35 g, 84%) as white solid of melting point of 86-88° C.

후처리

  1. customThe autoclave was sealed
  2. custompurged with hydrogen
  3. custompurged with nitrogen
  4. filtrationThe reaction mixture was filtered over diatomaceous earth
  5. concentrationthe filtrate was concentrated
  6. customThe residue was purified by chromatography

출처 및 근거

ORD 기록
ord-c365839b077a400bb5be74e6ab92efe5
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178540B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트