N-Iodosuccinimide → 7-iodo-2,4-bis-benzyloxy-5H-pyrrolo[3,2-d]pyrimidine

HRID 57785노트

반응식

HRID 57785 반응식
[CH2:1]([O:8][C:9]1[N:10]=[C:11]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:12]2[NH:17][CH:16]=[CH:15][C:13]=2[N:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1C(=O)N([I:33])C(=O)C1>C(Cl)Cl>[I:33][C:15]1[C:13]2[N:14]=[C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[N:10]=[C:11]([O:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:12]=2[NH:17][CH:16]=1

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 109255905H-Pyrrolo3,2-dpyrimidine, 2,4-bis(phenylmethoxy)-

생성물 1

HCID 718123077-iodo-2,4-bis-benzyloxy-5H-pyrrolo[3,2-d]pyrimidine수율 90.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 2,4-bis-O-benzyl-5H-pyrrolo[3,2-d]pyrimidine 15 (1.43 g, 4.3 mmol) in anhydrous CH2Cl2 (15 mL) under N2, NIS (1.069 g, 4.7 mmol) was added at which point the reaction mixture turned from pink to orange. The mixture was stirred overnight until the TLC indicated the absence of starting material. The reaction mixture was washed with aqueous Na2S2O3 (15 mL) followed by brine (15 mL). The organic layer was dried over MgSO4, loaded onto silica and purified using column chromatography eluting with 4:1 then 1:1 hexanes/EtOAc to obtain compound 16 as a pale-yellow solid (1.77 g, 3.88 mmol, 90%). Rf 0.4 in 1:3 hexanes/EtOAc. Mp 157.8-158.4° C. 1H NMR (400 MHz, CDCl3): δ 5.53 (s, 4H), 7.32-7.41 (m, 9H), 7.55-7.57 (m, 2H), 8.71 (br s, 1H, NH). 13C NMR: 57.3, 68.7, 69.3, 111.9, 127.9, 128.3, 128.6, 128.66, 128.7, 128.9, 132.4, 135.8, 137.2, 152.0, 156.9, 160.1. FAB-MS m/z for C20H16IN3O2 calculated [M+H]+ 458.0360. found 458.0357.

후처리

  1. washThe reaction mixture was washed with aqueous Na2S2O3 (15 mL)
  2. dry with materialThe organic layer was dried over MgSO4
  3. custompurified
  4. washeluting with 4:1

출처 및 근거

ORD 기록
ord-26985f8cc72d4e9cbc8579654c24fc41
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09434742B1

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