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

Hydrochloric Acid → HCID 66732179, 화합물

HRID 1963234
노트
인쇄 미리보기

반응식

HRID 1963234 반응식
[C:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][N:14]=1)[C:7]([O:9][CH2:10][CH3:11])=[O:8])(=[O:3])[NH2:2].[ClH:15]>CO.[Pt](=O)=O>[ClH:15].[C:1]([CH:4]1[CH2:5][CH:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:12][CH2:13][NH:14]1)(=[O:3])[NH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 11790073Ethyl 2-carbamoylisonicotinate

생성물 1

HCID 66732179HCID 66732179, 화합물수율 90%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매3회HCID 887Methanol용매2회

실험 절차

Ethyl 2-carbamoylisonicotinate (4.24 g, 21.83 mmol) was slurried in MeOH (50 mL) and HCl in MeOH (17.47 mL, 21.83 mmol) and platinum(IV) oxide (0.248 g, 1.09 mmol) were added. The mixture was hydrogenated at 5 bar in a Büchi hydrogenation apparatus. After 3 h there were still starting material left. platinum(IV) oxide (0.14 g, 0.62 mmol) was added and the reaction continued for 2 h when platinum(IV) oxide (0.387 g, 1.70 mmol) was added and the reaction was stirred overnight. The reaction mixture was filtered and evaporated to give ethyl 2-carbamoylpiperidine-4-carboxylate hydrochloride (3.93 g, 90%). 1H NMR (400 MHz, dmso) δ 1.16 (t, 3H), 1.31-1.63 (m, 2H), 1.86 (d, 1H), 2.26 (d, 1H), 2.54-2.66 (m, 1H), 2.74-2.88 (m, 1H), 3.10-3.19 (m, 1H), 3.47-3.56 (m, 1H), 4.06 (q, 2H), 7.38 (s, 1H), 7.71 (s, 1H). MS m/z 201 (M+H)+

후처리

  1. waitmaterial left
  2. waitthe reaction continued for 2 h
  3. filtrationThe reaction mixture was filtered
  4. customevaporated

출처 및 근거

ORD 기록
ord-684d76cec9e149878a2c588733a223e8
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08415378B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트