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

Oxalyl chloride → 6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-methyl-3-(1,3-thiazol-2-yl)-1,2-benzoxazole-5-carbaldehyde

HRID 245503
노트
인쇄 미리보기

반응식

HRID 245503 반응식
C(Cl)(=O)C(Cl)=O.[CH3:7][C@H:8]1[O:13][C@@H:12]([CH3:14])[CH2:11][N:10]([C:15]2[C:28]([C:29](O)=[O:30])=[CH:27][C:18]3[C:19]([C:22]4[S:23][CH:24]=[CH:25][N:26]=4)=[N:20][O:21][C:17]=3[C:16]=2[CH3:32])[CH2:9]1.[H-].C(O[Al](OC(C)(C)C)OC(C)(C)C)(C)(C)C.[Li+]>CN(C=O)C.ClCCl>[CH3:7][C@H:8]1[O:13][C@@H:12]([CH3:14])[CH2:11][N:10]([C:15]2[C:28]([CH:29]=[O:30])=[CH:27][C:18]3[C:19]([C:22]4[S:23][CH:24]=[CH:25][N:26]=4)=[N:20][O:21][C:17]=3[C:16]=2[CH3:32])[CH2:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 65578Oxalyl chlorideHCID 16710494Lithium tri-tert-butoxyaluminohydrideHCID 673582146-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-methyl-3-(1,3-thiazol-2-yl)-1,2-benzoxazole-5-carboxylic acid2회

생성물 1

HCID 866581096-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-methyl-3-(1,3-thiazol-2-yl)-1,2-benzoxazole-5-carbaldehyde

시약·촉매·용매 2

HCID 6228
Dimethylformamide
촉매
HCID 6344Dichloromethane용매

실험 절차

Oxalyl chloride (0.31 g, 2.4 mmol) was added to a stirred solution of 6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-methyl-3-(1,3-thiazol-2-yl)-1,2-benzoxazole-5-carboxylic acid (Intermediate 326, 0.18 g, 0.4 mmol) and two drops DMF in dichloromethane (5 mL) at 0° C. and the mixture was stirred at room temperature for 2 hours. Solvent was removed under reduced pressure and the residue was dissolved in THF (10 mL) and the solution was cooled to −78° C. and 1M solution of lithium tri(t-butoxy)aluminum hydride (0.28 g, 1.1 mmol) was added slowly and it was stirred for 30 mins at the same temperature. The reaction was quenched with 1.5N hydrochloric acid and extracted with ethyl acetate, the combined organic layers were dried over sodium sulfate and the solvent was removed. The brown viscous oil thus obtained was purified by silica gel column chromatography (20% ethyl acetate in hexane) affording the product as yellow solid. Yield: 0.06 g (35%).

후처리

  1. customSolvent was removed under reduced pressure
  2. dissolutionthe residue was dissolved in THF (10 mL)
  3. temperaturethe solution was cooled to −78° C.
  4. stirringit was stirred for 30 mins at the same temperature
  5. customThe reaction was quenched with 1.5N hydrochloric acid
  6. extractionextracted with ethyl acetate
  7. dry with materialthe combined organic layers were dried over sodium sulfate
  8. customthe solvent was removed
  9. customThe brown viscous oil thus obtained
  10. customwas purified by silica gel column chromatography (20% ethyl acetate in hexane)

출처 및 근거

ORD 기록
ord-e76c0023c6344a9fa73cd60e58539b19
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658641B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트