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

Phenyl Isothiocyanate → (RS) 3-{5-[2-(2-Phenylamino-benzoxazol-6-yl)-acetylamino]-pyridin-2-yl}-butyric acid

HRID 49699
노트
인쇄 미리보기

반응식

HRID 49699 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([NH:11][C:12]2[CH:13]=[CH:14][C:15]([CH:18]([CH3:24])[CH2:19][C:20]([O:22]C)=[O:21])=[N:16][CH:17]=2)=[O:10])=[CH:4][C:3]=1[OH:25].[C:26]1([N:32]=[C:33]=S)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C(O)C>[C:26]1([NH:32][C:33]2[O:25][C:3]3[CH:4]=[C:5]([CH2:8][C:9]([NH:11][C:12]4[CH:13]=[CH:14][C:15]([CH:18]([CH3:24])[CH2:19][C:20]([OH:22])=[O:21])=[N:16][CH:17]=4)=[O:10])[CH:6]=[CH:7][C:2]=3[N:1]=2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7673Phenyl IsothiocyanateHCID 17946638(RS) Methyl 3-{5-[2-(4-amino-3-hydroxy-phenyl)-acetylamino]-pyridin-2-yl}-butanoate

생성물 1

HCID 9932413(RS) 3-{5-[2-(2-Phenylamino-benzoxazol-6-yl)-acetylamino]-pyridin-2-yl}-butyric acid

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
70 °C

실험 절차

A solution of (RS) methyl 3-{5-[2-(4-amino-3-hydroxy-phenyl)-acetylamino]-pyridin-2-yl}-butyrate (41.2 mg, Reference Example 24) in ethanol (1 mL) was treated with a solution of phenyl isothiocyanate (16.23 mg) in ethanol (2 mL). The mixture allowed to stand at room temperature for 48 hours, then heated at 70° C. for 16 hours and then evaporated. The residue, (RS) methyl 3-{5-[2-(3-hydroxy-4-(3-phenylthioureido)-phenyl)-acetylamino]-pyridin-2-yl}-butyrate, was dissolved in dry dimethylformamide (1 mL) and the solution was treated with a solution of dicyclohexylcarbodiimide (74.2 mg) in dry dimethylformamide (2 mL). This mixture was heated at 70° C. for 12 hours and then evaporated. The residue was dissolved in methanol (2 mL) and the solution was treated with aqueous sodium hydroxide (600 μL, 1M). After shaking for 24 hours the mixture was filtered and the filtrate was acidified with aqueous acetic acid (1 mL, 1M). The precipitate was filtered and dissolved in dimethylformamide. This solution was evaporated and the residue was subjected to reversed phase HPLC on a Hypersil Elite C18 column (100 mm×21 mm) using 0.05% TFA in acetonitrile water to give the title compound. LC-MS: RT=2.36 minutes; MS (ES+): 431 (MH+).

후처리

  1. customevaporated
  2. dissolutionThe residue, (RS) methyl 3-{5-[2-(3-hydroxy-4-(3-phenylthioureido)-phenyl)-acetylamino]-pyridin-2-yl}-butyrate, was dissolved in dry dimethylformamide (1 mL)
  3. additionthe solution was treated with a solution of dicyclohexylcarbodiimide (74.2 mg) in dry dimethylformamide (2 mL)
  4. temperatureThis mixture was heated at 70° C. for 12 hours
  5. customevaporated
  6. dissolutionThe residue was dissolved in methanol (2 mL)
  7. additionthe solution was treated with aqueous sodium hydroxide (600 μL, 1M)
  8. filtrationwas filtered
  9. filtrationThe precipitate was filtered
  10. dissolutiondissolved in dimethylformamide
  11. customThis solution was evaporated

출처 및 근거

ORD 기록
ord-f8d5ec0155544f74bdc4baec67ad2b40
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706738B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트