2,3-dideoxy-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose | 742102-79-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,3-dideoxy-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose
• 英文别名: tert-butyl N-[[(2S,5S,6R)-6-(hydroxymethyl)-5-phenylmethoxyoxan-2-yl]methyl]carbamate
• CAS: 742102-79-0
• 化学式: C₁₉H₂₉NO₅
• 分子量: 351.443
• InChiKey: IBJHRDGAUNLNOR-YESZJQIVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  25
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  77
• 氢给体数：
  2
• 氢受体数：
  5

上下游信息

• 上游原料

  中文名称	英文名称	CAS号	化学式	分子量
  ——	2,3-dideoxy-5,7-O-benzylidene-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose	742102-77-8	C19H27NO5	349.427
  ——	2,3-dideoxy-4-O-benzyl-6-O-triphenylmethyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose	742102-75-6	C38H43NO5	593.763
  ——	2,3-dideoxy-6-O-triphenylmethyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose	742102-73-4	C31H37NO5	503.638

• 下游产品

  中文名称	英文名称	CAS号	化学式	分子量
  ——	(1S,4S,5S)-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-tetrahydropyran-6-carboxylic acid	742102-82-5	C19H27NO6	365.426
  ——	(1S,4S,5S)-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}tetrahydropyran-6-N-L-leucine methyl ester	742102-86-9	C26H42N2O6	478.629
  ——	(1S,4S,5S)-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}tetrahydropyran-6-N-L-methionine methyl ester	742102-84-7	C25H40N2O6S	496.668
  ——	N-[(1S)-1-({N-[(tert-butoxy)carbonyl]amino}methyl)-1,2,3-trideoxy-4-benzyloxy-6-oxo-D-arabino-hexopyranos-6-yl]-L-leucine methyl ester	742102-94-9	C26H40N2O7	492.613
  ——	N-[(1S)-1-({N-[(tert-butoxy)carbonyl]amino}methyl)-1,2,3-trideoxy-4-benzyloxy-6-oxo-D-arabino-hexopyranos-6-yl]-L-methionine methyl ester	742102-96-1	C25H38N2O7S	510.652

反应信息

• 作为反应物：
  描述：

  2,3-dideoxy-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose 在 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 碘苯二乙酸 作用下， 以 二氯甲烷 为溶剂， 以85%的产率得到(1S,4S,5S)-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-tetrahydropyran-6-carboxylic acid
  参考文献：
  名称：

  Design, Synthesis, and Evaluation of Su- gar Amino Acid Based Inhibitors of Pro- tein Prenyl Transferases PFT and PGGT-1

  摘要：

  Eleven analogues of the C-terminal Ca(1)a(2)X Motif found in natural substrates of the prenyl transferases PFT and PGGT-1 were synthesized and evaluated for their inhibition potency and selectivity against PFT and PGGT-1. Replacement of the central dipeptide part a(1)a(2) by a benzylated sugar amino acid resulted in a good and highly selective PFT inhibitor (8, IC50 = 250 +/- 20 nM). The methyl ester of 8 (13) selectively inhibited protein farnesylation in cultured cells.

  DOI：

  10.1021/jm049927q
• 作为产物：
  描述：

  2,3-dideoxy-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose 在 二异丁基氢化铝 、 (+)-10-camphorsulfonic acid 作用下， 以 甲苯 、 乙腈 为溶剂， 反应 2.5h， 生成 2,3-dideoxy-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-α-D-glucopyranose
  参考文献：
  名称：

  Design, Synthesis, and Evaluation of Su- gar Amino Acid Based Inhibitors of Pro- tein Prenyl Transferases PFT and PGGT-1

  摘要：

  Eleven analogues of the C-terminal Ca(1)a(2)X Motif found in natural substrates of the prenyl transferases PFT and PGGT-1 were synthesized and evaluated for their inhibition potency and selectivity against PFT and PGGT-1. Replacement of the central dipeptide part a(1)a(2) by a benzylated sugar amino acid resulted in a good and highly selective PFT inhibitor (8, IC50 = 250 +/- 20 nM). The methyl ester of 8 (13) selectively inhibited protein farnesylation in cultured cells.

  DOI：

  10.1021/jm049927q