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

HCID 67264659, 화합물 → HCID 67263426, 화합물

HRID 1687254
노트
인쇄 미리보기

반응식

HRID 1687254 반응식
[CH3:1][N:2]1[C:8]2[C:9]([N+:13]([O-])=O)=[CH:10][CH:11]=[CH:12][C:7]=2[C:6](=[O:16])[NH:5][CH2:4][CH2:3]1>CO.[Pd]>[NH2:13][C:9]1[C:8]2[N:2]([CH3:1])[CH2:3][CH2:4][NH:5][C:6](=[O:16])[C:7]=2[CH:12]=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 67264659HCID 67264659, 화합물

생성물 1

HCID 67263426HCID 67263426, 화합물수율 99.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

1-Methyl-9-nitro-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one (#) (100 mg, 0.45 mmol) was dissolved in MeOH (20 ml) and placed in a Parr bottle. Pd—C (10%, 10 mg) was added, and the resulting mixture was shaken under 20 psi H2 for 1.5 h. The reaction mixture was filtered through celite, washed with MeOH, and concentrated to afford 9-Amino-1-methyl-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one as a brown solid (86 mg, 99%). mp 130-133° C.; LCMS: m/z=192.30 (M+H+); 1H NMR (400 MHz, CDCl3) δ 7.26 (m, 1H), 6.80 (m, 2H), 3.79 (bs, 2H), 3.45 (m, 4H), 3.16 (s, 3H).

후처리

  1. filtrationThe reaction mixture was filtered through celite
  2. washwashed with MeOH
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f877890695e645f68880a29f2a62720b
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148391B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트