2,2,2-trichloroethyloxycarbonylhydrazine | 31434-96-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 2,2,2-trichloroethyloxycarbonylhydrazine
• 英文别名: 2,2,2-trichloroethyl carbazate；2,2,2-Trichloroethyl hydrazinecarboxylate；2,2,2-trichloroethyl N-aminocarbamate
• CAS: 31434-96-5
• 化学式: C₃H₅Cl₃N₂O₂
• 分子量: 207.444
• InChiKey: AKYVQEQYVJSLGN-UHFFFAOYSA-N

物化性质

• 沸点：
  299.6±40.0 °C(Predicted)
• 密度：
  1.617±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  10
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  64.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  Boc-L-蛋氨酸 、 2,2,2-trichloroethyloxycarbonylhydrazine 在 N,N'-二环己基碳二亚胺 作用下， 以 乙酸乙酯 为溶剂， 以88%的产率得到Boc-Met-NH-NH-Troc
  参考文献：
  名称：

  Diaz, Joseph; Guegan, Remy; Muneaux, Yvette, Bulletin de la Societe Chimique de France, 1989, # 4, p. 493 - 510

  摘要：

  DOI：
• 作为产物：
  描述：

  氯甲酸-2,2,2-三氯乙酯 在 一水合肼 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 2,2,2-trichloroethyloxycarbonylhydrazine
  参考文献：
  名称：

  电化学促进醛和氨基甲酸酯的环化：获得 2-烷氧基/芳氧基-5-取代的 1,3,4-恶二唑和 1,3,4-恶二唑-2(3H)-one 衍生物

  摘要：

  通过醛的环化，开发了一种高效且环保的化学和药学上有趣的 2-烷氧基/芳氧基-1,3,4-恶二唑和 1,3,4-恶二唑-2(3 H )-酮的合成方法和卡巴酸盐。该协议涉及以电化学方式促进以良好至优异的产量获得所需产品。该方法使用 NaBr 作为电催化剂，MeOH 作为溶剂。该策略不含氧化剂和过渡金属，可在室温下无电解质完成反应。基于对照实验结果和文献报道提出了一种可能的机制。通过5-(4-chloro-3-(trifluoromethyl)phenyl)-1,3,4-oxadiazol-2( 3 H)-one，它是 Notum 羧酸酯酶活性的有效抑制剂。

  DOI：

  10.1039/d2nj04113h

文献信息

• Synthesis of the octadecapeptide corresponding to positions 32 to 49 of the revised amino acid sequence of thymopoietin II and its effect on low E-rosette forming cells of an aged patient with chronic renal failure.
  作者：TAKASHI ABIKO、HIROSHI SEKINO

  DOI：10.1248/cpb.30.3271

  日期：——

  The octadecapeptide, H-Arg-Lys-Asp-Val-Tyr-Val-Glu-Leu-Tyr-Leu-Gln-Ser-Leu-Thr-Ala-Leu-Lys-Arg-OH, corresponding to positions 32 to 49 of the revised amino acid sequence of bovine thymopoietin II was synthesized by the azide condensation of three fragments, (32-36), (37-41) and (42-49), followed by deprotection with hydrogen fluoride in the presence of anisole-thioanisole-o-cresol. The in vitro addition of the synthetic thymopoietin II (32-49) significantly restored the low E-rosette forming capacity of cells from an aged patient with chronic renal failure to normal levels. The in vitro effect of [Gln38, Thr43, Val47]-thymopoietin II (32-49) on the low E-rosette forming capacity of cells from the aged patient with chronic renal failure was also compared with that of the synthetic thymopoietin II (32-49). The [Gln38, Thr43, Val47]-thymopoietin II (32-49) was approximately equipotent with the synthetic thymopoietin II (32-49) at a concentration of 100 μg/ml.

  十八肽H-Arg-Lys-Asp-Val-Tyr-Val-Glu-Leu-Tyr-Leu-Gln-Ser-Leu-Thr-Ala-Leu-Lys-Arg-OH，对应于牛胸腺生成素II修订后的氨基酸序列的第32至49位，通过三个片段(32-36)、(37-41)和(42-49)的叠氮化物缩合合成，随后在茴香硫醚-邻甲酚存在下用氢氟酸脱保护。体外添加合成的胸腺生成素II(32-49)显著恢复了来自慢性肾衰竭老年患者的细胞的低E玫瑰花形成能力至正常水平。[Gln38, Thr43, Val47]胸腺生成素II(32-49)对来自慢性肾衰竭老年患者的细胞的低E玫瑰花形成能力的影响也与合成的胸腺生成素II(32-49)进行了比较。在100 μg/ml的浓度下，[Gln38, Thr43, Val47]胸腺生成素II(32-49)与合成的胸腺生成素II(32-49)大致等效。
• A study on endocrine disorder in patients with chronic renal failure. I. Synthesis and biological activity of human gastrin I.
  作者：TAKASHI ABIKO、IKUKO ONODERA、HIROSHI SEKINO

  DOI：10.1248/cpb.30.2604

  日期：——

  A heptadecapeptide amide, H-Pyr-Gly-Pro-Trp-Leu-Glu-Glu-Glu-Glu-Glu-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH2, corresponding to the entire amino acid sequence of human gastric I, was synthesized by the solution method. This peptide inhibited lactate dehydrogenase activity by 87.6% at a concentration of 300 pg/ml. This peptide was tested for suppression of PHA-induced lymphocyte proliferation, but showed no significant activity.

  一种十七肽酰胺H-Pyr-Gly-Pro-Trp-Leu-Glu-Glu-Glu-Glu-Glu-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH2，对应于人胃泌素I的整个氨基酸序列，通过溶液法合成。该肽在300 pg/ml的浓度下抑制乳酸脱氢酶活性达87.6%。该肽被测试用于抑制PHA诱导的淋巴细胞增殖，但未显示出显著活性。
• Studies on peptides. CXXVII. Synthesis of a tripentacontapeptide with epidermal growth factor activity.
  作者：KENICHI AKAJI、NOBUTAKA FUJII、HARUAKI YAJIMA、KYOZO HAYASHI、KAZUHIKO MIZUTA、MITSURU AONO、MOTOYUKI MORIGA

  DOI：10.1248/cpb.33.184

  日期：——

  The tripentacontapeptide corresponding to the entire linear sequence of epidermal growth factor was synthesized by assembling 15 peptide fragments and one His residue (position 22), followed by deprotection with trifluoromethanesulfonic acid-thioanisole in trifluoroacetic acid. The deprotected peptide was subjected to air-oxidation. After purification by ion-exchange chromatography on diethyl aminoethyl cellulose followed by high performance liquid chromatography, a peptide with powerful anti-gastric activity was obtained.

  通过组装15个肽片段和一个组氨酸残基（位置22），合成了对应于表皮生长因子整个线性序列的三十五肽。随后，通过三氟甲磺酸-噻吩在三氟乙酸中进行脱保护。脱保护的肽进行空气氧化。经过二乙氨基乙基纤维素上的离子交换色谱法纯化，接着用高效液谱法，获得了一种具有强大抗胃活性的肽。
• Catalytic Enantioselective Amination of Enolsilanes Using <i>C</i><i>₂</i>-Symmetric Copper(II) Complexes as Chiral Lewis Acids
  作者：David A. Evans、Douglas S. Johnson

  DOI：10.1021/ol990113r

  日期：1999.8.1

  [formula: see text] [Cu(S,S)-t-Bu-box](OTf)2 (1) catalyzes the enantioselective amination of enolsilanes with azodicarboxylate derivatives. Isomerically pure enolsilanes of aryl ketones, acylpyrroles, and thioesters added to the azo-imide in greater than 95% ee. The use of an alcohol additive was critical to achieving catalyst turnover.

  [Cu：S（S，S）-t-Bu-box]（OTf）2（1）催化用偶氮二羧酸酯衍生物对烯醇硅烷的对映选择性胺化。芳族酮，酰基吡咯和硫代酸酯的异构纯烯醇硅烷以大于95％ee的量添加到偶氮酰亚胺中。醇添加剂的使用对于实现催化剂周转至关重要。
• Studies on peptides. CIX. Synthesis of the octatriacontapeptide corresponding to positions 1 to 38 of human parathyroid hormone.
  作者：SUSUMU FUNAKOSHI、NOBUTAKA FUJII、HARUAKI YAJIMA、CHOHEI SHIGENO、ITSUO YAMAMOTO、RIKUSHI MORITA、KANJI TORIZUKA

  DOI：10.1248/cpb.30.1706

  日期：——

  The octatriacontapeptide corresponding to positions 1 to 38 of human parathyroid hormone (hPTH), a half of the whole molecule, was synthesized by assembling 9 peptide fragments in a conventional manner. Arg (mesitylene-2-sulfonyl), a new arginine derivative bearing an acid-labile protecting group, was employed in combination with a new deprotecting procedure with 1 M trifluoromethanesulfonic acid-thioanisole in TFA. The synthetic peptide exhibited an activity of 1400 IU/mg when assayed by the mouse bone adenyl cyclase activity assay.

  合成人类甲状旁腺激素（hPTH）第1到第38位的八三十肽，通过传统方法组装9个肽片段合成。使用了一种新型的精氨酸衍生物Arg（美克辛烯-2-磺酸），该衍生物具有一种酸敏感的保护基团，并结合了使用1 M三氟甲烷磺酸-硫代苯醚在TFA中进行的新脱保护工艺。合成的肽在小鼠骨腺苷酸酰化酶活性测定中表现出1400 IU/mg的活性。