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

Morpholine → HCID 67287001, 화합물

HRID 922022
노트
인쇄 미리보기

반응식

HRID 922022 반응식
Cl[C:2]1[N:7]=[C:6]([S:8][CH2:9][CH3:10])[C:5]([C:11]([O:13][CH3:14])=[O:12])=[C:4]([C:15]([F:18])([F:17])[F:16])[CH:3]=1.C(SC1C(C(OC)=O)=C(C(F)(F)F)C=C(SCC)N=1)C.[NH:39]1[CH2:44][CH2:43][O:42][CH2:41][CH2:40]1.CCN(C(C)C)C(C)C>CC#N.O.CCOC(C)=O>[CH2:9]([S:8][C:6]1[C:5]([C:11]([O:13][CH3:14])=[O:12])=[C:4]([C:15]([F:18])([F:17])[F:16])[CH:3]=[C:2]([N:39]2[CH2:44][CH2:43][O:42][CH2:41][CH2:40]2)[N:7]=1)[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 8083MorpholineHCID 81531DiisopropylethylamineHCID 67288028HCID 67288028, 화합물HCID 86664318HCID 86664318, 화합물

생성물 1

HCID 67287001HCID 67287001, 화합물수율 16%

시약·촉매·용매 3

HCID 962Water용매
HCID 6342
Acetonitrile
용매
HCID 8857Ethyl Acetate용매

반응 조건

온도
150 °C

실험 절차

A solution of 2 g of a ˜1:1 mixture of methyl 6-chloro-2-(ethylsulfanyl)-4-(trifluoromethyl)-pyridine-3-carboxylate and methyl 2,6-bis(ethylsulfanyl)-4-(trifluoromethyl)-pyridine-3-carboxylate, 1.7 ml (20.0 mmol) morpholine and 3.5 ml (20.0 mmol) DIPEA in MeCN (10 ml) was heated in the microwave to 150° C. for 4 h. The RM was then diluted with water and EtOAc. The organic layer was separated, washed with water and brine, dried over MgSO4 and concentrated in vacuo. Purification of the residue by CC (hexane/EtOAc 4:1) provided 440 mg (1.3 mmol, 16% over 2 steps) methyl 2-(ethylsulfanyl)-6-morpholin-4-yl-4-(trifluoromethyl)-pyridine-3-carboxylate.

후처리

  1. customThe organic layer was separated
  2. washwashed with water and brine
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated in vacuo
  5. customPurification of the residue by CC (hexane/EtOAc 4:1)

출처 및 근거

ORD 기록
ord-16ad6f99a2834f5fb83214103e01a9e8
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278103B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트