Acetic Acid 5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl Ester → Acetic Acid 4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-5-hydroxymethyl-tetrahydro-furan-3-yl Ester

HRID 1645301

反応式

HRID 1645301 の反応式
COC1C=CC(C(C2C=CC(OC)=CC=2)[O:10][CH:11](C2C=CC=CC=2)[CH:12]2[O:16][CH:15]([N:17]3[CH:22]=[CH:21][C:20](=[O:23])[NH:19][C:18]3=[O:24])[CH:14]([O:25][C:26](=[O:28])[CH3:27])[CH:13]2[O:29][Si:30]([C:43]([CH3:46])([CH3:45])[CH3:44])([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)=CC=1>C(O)(=O)C>[C:43]([Si:30]([C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)([C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1)[O:29][CH:13]1[CH:12]([CH2:11][OH:10])[O:16][CH:15]([N:17]2[CH:22]=[CH:21][C:20](=[O:23])[NH:19][C:18]2=[O:24])[CH:14]1[O:25][C:26](=[O:28])[CH3:27])([CH3:44])([CH3:45])[CH3:46]

参加物

3

実験手順

The 5′-O-DMT group is removed as per known literature procedures 4,4′-dimethoxytrityl ethers are commonly removed under acidic conditions (Oligonucleotides and analogues, A Practical Approach, Eckstein, F., ed, IRL Press, New York.) Generally, Compound 8 (1 eq.) is dissolved in 80% aqueous acetic acid. After several hours, the mixture is evaporated, dissolved in ethyl acetate and washed with a sodium bicarbonate solution. Purification by silica gel chromatography will give compound 9.

後処理

  1. customThe 5′-O-DMT group is removed as
  2. customare commonly removed under acidic conditions (Oligonucleotides and analogues
  3. waitAfter several hours
  4. customthe mixture is evaporated
  5. dissolutiondissolved in ethyl acetate
  6. washwashed with a sodium bicarbonate solution
  7. customPurification by silica gel chromatography

出典と根拠

ORDレコード
ord-2fd374dff5a34881b00c09bc4a7332fb
出典データセット
uspto-grants-2012_02
特許番号
US08124745B2

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