N-Iodosuccinimide → N4-(Cyclopropylmethyl)-5-iodopyrimidine-2,4-diamine

HRID 79146노트

반응식

HRID 79146 반응식
[I:1]N1C(=O)CCC1=O.[CH:9]1([CH2:12][NH:13][C:14]2[CH:19]=[CH:18][N:17]=[C:16]([NH2:20])[N:15]=2)[CH2:11][CH2:10]1>CC(O)=O>[CH:9]1([CH2:12][NH:13][C:14]2[C:19]([I:1])=[CH:18][N:17]=[C:16]([NH2:20])[N:15]=2)[CH2:10][CH2:11]1

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 20277654N4-(cyclopropylmethyl)pyrimidine-2,4-diamine

생성물 1

HCID 58299566N4-(Cyclopropylmethyl)-5-iodopyrimidine-2,4-diamine수율 60%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
80 °C

실험 절차

N-iodosuccinimide (11.5 g, 50.9 mmol) was added to a solution of compound 237 (7.60 g, 46.3 mmol) in AcOH (90 mL). The reaction was warmed to 80° C. and stirred for 1.5 h. Solvent was removed in vacuo. The residue was taken up in dichloromethane (200 mL) and water. The aqueous layer was brought to pH 12 with 5 N NaOH and organics were sequestered. The aqueous was extracted further with dichloromethane (2×100 mL). The combined organics were treated with solid sodium thiosulfate, dried with MgSO4 and concentrated in vacuo. Silica gel chromatography (gradient elution 10 to 75% ethyl acetate in hexanes) afforded compound 238 (8.0 g, 60% yield).

후처리

  1. customSolvent was removed in vacuo
  2. extractionThe aqueous was extracted further with dichloromethane (2×100 mL)
  3. additionThe combined organics were treated with solid sodium thiosulfate
  4. dry with materialdried with MgSO4
  5. concentrationconcentrated in vacuo
  6. washSilica gel chromatography (gradient elution 10 to 75% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-bf5e72b479724e449a607398db936fdd
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841312B2

반응 노트

불러오는 중…