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

HCID 86636687, 화합물 → tert-Butyl {[1-(2-aminoethyl)piperidin-4-yl]methyl}carbamate

HRID 1046560
노트
인쇄 미리보기

반응식

HRID 1046560 반응식
[C:1]([CH2:3][N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][NH:11][C:12](=[O:18])[O:13][C:14]([CH3:17])([CH3:16])[CH3:15])[CH2:6][CH2:5]1)#[N:2]>CO.[Ni]>[NH2:2][CH2:1][CH2:3][N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][NH:11][C:12](=[O:18])[O:13][C:14]([CH3:16])([CH3:15])[CH3:17])[CH2:6][CH2:5]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86636687HCID 86636687, 화합물

생성물 1

HCID 34178247tert-Butyl {[1-(2-aminoethyl)piperidin-4-yl]methyl}carbamate

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

To a hydrogenation flask charged with a solution of tert-butyl (1-(cyanomethyl)piperidin-4-yl)methylcarbamate (5.4 g, 21.3 mmol) in CH3OH (20 mL) was added Raney nickel (˜1 g, rinsed with CH3OH). The flask was shaken at room temperature under hydrogen (40 psi) overnight. The reaction mixture was then filtered through a celite cake, and the filtrate was concentrated to give sticky foam which was used in the next step without further purification.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • filtrationThe reaction mixture was then filtered through a celite cake
  • concentrationthe filtrate was concentrated
  • customto give sticky foam which
  • customwas used in the next step without further purification
  • 출처 및 근거

    ORD 기록
    ord-8df4f78dee974693923d348c5a3e3f4e
    출처 데이터셋
    uspto-grants-2013_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08569344B2

    반응 노트

    불러오는 중…