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

Methanol → HCID 22561682, 화합물

HRID 1839674
노트
인쇄 미리보기

반응식

HRID 1839674 반응식
O[O:2][S:3]([O-:5])=O.[K+].C([O:9][C:10]([C:12]1[C:16]([CH2:17][CH2:18][CH2:19]SC)=[C:15]([CH:22]=[O:23])[NH:14][C:13]=1[CH3:24])=[O:11])C.[CH3:25]O>O>[CH:22]([C:15]1[NH:14][C:13]([CH3:24])=[C:12]([C:10]([OH:11])=[O:9])[C:16]=1[CH2:17][CH2:18][CH2:19][S:3]([CH3:25])(=[O:5])=[O:2])=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 20761747HCID 20761747, 화합물HCID 23707502Potassium hydroxy sulfite

생성물 1

HCID 22561682HCID 22561682, 화합물

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

Oxone (614 mg, 1 mmol) dissolved in water (2 mL) was added portionwise to a solution of 5-formyl-2-methyl-4-(3-methylsulfanyl-propyl)-1H-pyrrole-3-carboxylic acid ethyl ester (269 mg, 1 mmol) in methanol (4 mL) cooled in an ice bath. The mixture was stirred for 3 hours, keeping the temp between 0° C. and rt. The reaction was diluted with 10 mL of water, the resulted precipitate was collected by vacuum filtration, washed with water and dried to give 95 mg of the desired product. The water filtrate was extracted with ethyl acetate, dried and concentrated to give another 74 mg of the product. Total of 169 mg (56%) of 5-formyl-4-(3-methanesulfonyl-propyl)-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester was obtained.

후처리

  1. temperaturecooled in an ice bath
  2. customthe temp between 0° C. and rt
  3. filtrationthe resulted precipitate was collected by vacuum filtration
  4. washwashed with water
  5. customdried

출처 및 근거

ORD 기록
ord-94460a2f39fa4a559194c3da86ce8d4d
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06677368B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트