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

Triethylamine → Cefotaxime

HRID 362590
노트
인쇄 미리보기

반응식

HRID 362590 반응식
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:11]/[O:12][CH3:13])/[C:8]([OH:10])=O)[N:6]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:33][C:34]([O:36][CH2:37][C:38]1[CH2:47][S:46][C@@H:41]2[C@H:42]([NH2:45])[C:43](=[O:44])[N:40]2[C:39]=1[C:48]([OH:50])=[O:49])=[O:35].C(N(CC)CC)C>O1CCCC1.CN(C)C(=O)C.O.C(O)(=O)C>[CH3:33][C:34]([O:36][CH2:37][C:38]1[CH2:47][S:46][C@@H:41]2[C@H:42]([NH:45][C:8](/[C:7](/[C:5]3[N:6]=[C:2]([NH2:1])[S:3][CH:4]=3)=[N:11]\[O:12][CH3:13])=[O:10])[C:43](=[O:44])[N:40]2[C:39]=1[C:48]([OH:50])=[O:49])=[O:35]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 4

HCID 8471TriethylamineHCID 11776TriphenylphosphineHCID 4413287-Aminocephalosporanic acidHCID 5486924(alphaZ)-2-Amino-alpha-(methoxyimino)-4-thiazoleacetic acid

생성물 1

HCID 5742673Cefotaxime

시약·촉매·용매 4

HCID 176Acetic Acid용매
HCID 962Water용매2회
HCID 8028Tetrahydrofuran용매
HCID 31374Dimethylacetamide용매

실험 절차

2,2'-Dithio-bis-5-methyl-1,3,4-thiadiazole (48.09 g) and (Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetic acid (23.38 g) were suspended in tetrahydrofuran (297 ml) and triphenylphosphine (48.09) was added at 20°-25° C. This mixture was stirred for half an hour to generate 2-mercapto-5-methyl-1,3,4-thiadiazolyl-(Z)-2-(2-aminothiazol-4-yl)-2-methoxyimino acetate in solution. Thereafter, the reaction mixture was cooled to 3°-5° C., diluted with N,N-dimethylacetamide (46.8 ml), water (297 ml) and 7-aminocephalosporanic acid (27.2 g) was added, followed by triethylamine addition in 20 min. The reaction was continued for 3-4 hours at 3°-5° C. Thereafter, acetic acid (18 g) and water (100 ml) were added and the aqueous layer was thoroughly extracted with methylene chloride to remove tetrahydrofuran and other by-products. The aqueous phase containing triethylamine salt of cefotaxime acid was mixed with excess isopropyl alcohol (250 ml) and acidified to pH 2.80 at 0°-5°° C. with hydrochloric acid to precipitate cefotaxime acid. The mixture was then filtered, the solids washed with water, isopropyl alcohol and dried to obtain cefotaxime acid.

후처리

  1. temperatureThereafter, the reaction mixture was cooled to 3°-5° C.
  2. additionwas added
  3. extractionthe aqueous layer was thoroughly extracted with methylene chloride
  4. customto remove tetrahydrofuran and other by-products
  5. additionThe aqueous phase containing triethylamine salt of cefotaxime acid
  6. additionwas mixed with excess isopropyl alcohol (250 ml)
  7. customacidified to pH 2.80 at 0°-5°° C
  8. customwith hydrochloric acid to precipitate cefotaxime acid
  9. filtrationThe mixture was then filtered
  10. washthe solids washed with water, isopropyl alcohol
  11. customdried

출처 및 근거

ORD 기록
ord-6b1ea39a5b6c4a2999cf84051403682a
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05869649

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트