ÌÚ²©tengbo9885¹ÙÍø

ÐÂÎŶ¯Ì¬

°±»ù±£»¤»ù¡ªÈý±½¼×»ùϵÁÐ
·ÖÀà £ºÐÂÎÅ
Ðû²¼Ê±¼ä £º2025/07/11
»á¼ûÁ¿ £º1

°±»ùÊdz£¼ûµÄ»îÐÔ»ùÍÅ£¬ÔÚ·´Ó¦ÖÐÍùÍùÐèÒªÊÂÏȱ£»¤ ¡£Æä±£»¤»ùÖÖÀà·±¶à£¬´ËǰÒÑÏÈÈÝÁËõ£»ùϵÁеı£»¤»ù£¬±¾ÎÄ×îÏȽ«ÏÈÈÝÍé»ùÀà±£»¤»ù ¡£


Èý±½¼×»ùϵÁб£»¤»ùÊÇÒ»Àà¿Õ¼äλ×è½Ï´óµÄ±£»¤»ù£¬ÒýÈëºÍÍѳýÌõ¼þÎÂ˳£¬²Ù×÷ÇáÓ¯£¬ÆäÎȹÌÐԸߣ¬ÌØÊâÊÊÓÃÓÚ¶à¹ÙÄÜÍÅ»¯ºÏÎïµÄÑ¡ÔñÐÔ±£»¤ ¡£±ðµÄ£¬Èý±½¼×»ùϵÁб£»¤»ùµÄÒýÈëÓÐÖúÓÚ»¯ºÏÎïÐγɾ§Ì壬Ò×ͨ¹ý½á¾§·¨Ìá´¿ ¡£


¼ò½é



³£¼ûµÄÈý±½¼×»ùϵÁб£»¤»ùÖ÷Òª°üÀ¨£ºÈý±½¼×»ù£¨Trt£©£¬4-¼×Ñõ»ùÈý±½¼×»ù£¨MMT£©£¬4,4'-Ë«¼×Ñõ»ùÈý±½¼×»ù£¨DMT£©£¬4,4',4''-Èý¼×Ñõ»ùÈý±½¼×»ù£¨TMT£©£¨Í¼1£©£¬¸ÃϵÁб£»¤»ùÔÚ¼îÐÔÌõ¼þ»òÇ׺ËÊÔ¼Á±£´æÏ½ÏÁ¿ÎȹÌ£¬µ«ÔÚËáÐÔÌõ¼þÏÂÒ×±»Íѳý£¬ÆäÔÚËáÐÔÌõ¼þϵÄÍѳý»îÐÔΪTMT>DMT>MMT>Trt ¡£¼øÓÚ¸ÃϵÁб£»¤»ùµÄÒýÈëºÍÍѳýÒªÁì»ùÄÚÇéËÆ£¬±¾ÎÄ×ÅÖØÒÔTrtΪÀý¾ÙÐÐÏÈÈÝ ¡£


ͼ1ÌÚ²©tengbo9885_Ê×Ò³(»¶Ó­Äú)

ͼ1 ³£¼ûµÄÈý±½¼×»ùϵÁб£»¤»ù½á¹¹


ÒýÈëÒªÁì



ÓÉÓÚλ×è½Ï´ó£¬Èý±½¼×»ùϵÁб£»¤»ùͨ³£ÓÃÓÚ±£»¤²®°·£¬Æä¹¦Ð§ÓëÈý·úÒÒËáÒÒõ¥¡¢N-ÒÒÑõôÊ»ùÁÚ±½¶þ¼×õ£Ñǰ·ÀàËÆ£¬¿ÉʵÏÖ²®°·µÄÑ¡ÔñÐÔ±£»¤ ¡£±ðµÄ£¬ÔÚ¶àëĺϳÉÖУ¬Èý±½¼×»ù±£»¤ÄÜÓÐÓÃÒÖÖÆ·´Ó¦Àú³ÌÖеÄÏûÐý»¯£¬ÓÈÆäÊÊÓÃÓÚº¬×é°±ËáµÄ¶àëÄ ¡£


Trt±£»¤»ùͨ³£ÔÚ¼îÐÔÌõ¼þϽÓÄÉTrt-Cl¾ÙÐз´Ó¦£¬ÕâÊÇ×î³£ÓõÄÒýÈëÒªÁìÖ®Ò»£¬ÆäËûÒªÁ컹°üÀ¨Trt-OH£¨Èý±½¼×´¼£©ºÍAc2OÔÚËáÐÔÌõ¼þϾÙÐУ¬»ò½ÓÄÉTMSCl/Et3N/Trt-ClµÄ×éºÏÒýÈëÈý±½¼×»ù£¬ÊµÀýÈçͼ2£º


ͼ2ÌÚ²©tengbo9885_Ê×Ò³(»¶Ó­Äú)

ͼ2 Èý±½¼×»ùÒýÈëʵÀý


ÍѳýÒªÁì



Ö»¹ÜÈý±½¼×»ùµÄÎȹÌÐÔ½ÏÁ¿¸ß£¬È´ÊÇËáÃô¸Ð»ùÍÅ£¬ÔÚ¶àÖÖËáÐÔÌõ¼þϺÜÈÝÒ×Íѳý£¬ÈçÑÎËáϵͳ¡¢TFA¡¢´×ËáµÈ ¡£Boc±£»¤»ùͨ³£Ò²ÊÇÔÚËáÐÔÌõ¼þÏÂÍѳý£¬¹Ê¿ÉÒÀ¾Ý²î±ð±£»¤»ù¶ÔËáÃô¸ÐµÄ²î±ð¾ÙÐÐÑ¡ÔñÐÔÍѳý£¬ÀýÈ磺ÔÚ50%HOAcË®ÈÜÒºÖУ¬¿ÉÒÔºÜÈÝÒ×ÍѳýTrt£¬¶øBoc±£»¤»ù²»ÊÜÓ°Ïì ¡£SieberµÈÈË¿¼²ìÁËTrt-His(Trt)-Lys(Boc)-OMeÖÐTrt¡¢Boc±£»¤»ùµÄÎȹÌÐÔ£¨Í¼3£©£¬·¢Ã÷×é°±Ëá²àÁ´µÄTrt±£»¤»ùÒª±È¦Á-°±»ùÉϵÄTrt¸üÎȹÌ£¬²¢ÇÒ£¬ÔÚ1 N HCl/´×ËáϵͳÄÚ£¬Boc»á±»ÍÑÈ¥¶ø×é°±Ëá²àÁ´µÄTrt²»ÊÜÓ°Ïì ¡£

ÌÚ²©tengbo9885_Ê×Ò³(»¶Ó­Äú)

ͼ3

ͼ3  Trt-His(Trt)-Lys(Boc)-OMeÖÐTrt¡¢Boc±£»¤»ùµÄÎȹÌÐÔ̽ÌÖ


³ý´ËÖ®Í⣬Èý±½¼×»ù»¹¿ÉÒÔͨ¹ýÒÔÏÂÒªÁìÍѱ£»¤£º

1. »¹Ô­Íѳý

¿ÉÔÚPd/CÇ⻯£¨ÏÂͼ£©¡¢Na/NH3(l)µÈ»¹Ô­Ìõ¼þÏÂÍÑÈ¥Trt±£»¤»ù ¡£ÆäÖУ¬ÔÚ´ß»¯Ç⻯Ìõ¼þÏ£¬TrtµÄÍѳýËÙÂÊÏÔÖøµÍÓÚO-Bn¡¢N-CbzµÈ±£»¤»ù£¬¹Ê¿ÉÒÔÆ¾Ö¤²î±ð±£»¤»ùµÄÌØÕ÷¾ÙÐÐÑ¡ÔñÐÔÍѳý ¡£


ͼ4

ͼ4 Pd/C´ß»¯Ç⻯ÍÑTrt


ÁíÍ⣬ChandrasekharÍŶӿª·¢ÁËÒ»ÖÖ½«N-Trt±£»¤Ò»²½×ª»¯ÎªN-Boc±£»¤µÄÒªÁ죬ͨ¹ýPd(OH)2/C¡¢PMHS£¨¾Û¼×»ùÇâ¹èÑõÍ飩µÄ×÷ÓÃÏ£¬ÊµÏÖµ¥²½ºÏ³ÉN-Boc»¯ºÏÎЧÂʸߣ¬µ×Îï¹æÄ£¹ã ¡£


ͼ5

ͼ5 Ò»²½·¨ºÏ³ÉN-Boc±£»¤


2. ·Ò×˹ËáÍѳý

¹ØÓÚ¶ÔÖ¤×ÓËáÃô¸ÐµÄµ×Î·Ò×˹ËáÈçZnBr2£¬BF3¡¤Et2OµÈÊÇÓÐÓõÄÍѱ£»¤ÊÔ¼Á ¡£ÀýÈ磬ÔÚBF3¡¤Et2O/Me3SiH/HFIP£¨Áù·úÒì±û´¼£©ÏµÍ³ÄÚ¿ÉÒÔ¿ìËÙ£¬¸ßЧÍѳý ¡£


ͼ6

ͼ6 ·Ò×˹ËáÍÑMMT


3.CAN£¨ÏõËáîæï§£©ÊÔ¼ÁÍѳý

CANÊÔ¼Á¿ÉÒÔͨ¹ýµ¥µç×Ó×ªÒÆµÄ·½·¨ÍѳýTrt£¬´Ó¶ø°±»ùת±äΪ°±»ù¸ºÀë×Ó£¬Àú³ÌÖÐÐèÒª´×ËáµÈÌṩÇâÖÊ×ӲŻª»ñµÃÓÎÀë°·£¬²»È»»áÖØÐÂÌìÉúÖÊÁÏ ¡£

ÌÚ²©tengbo9885_Ê×Ò³(»¶Ó­Äú)

ͼ7

ͼ7 CANÊÔ¼ÁÍÑTrt


Èý±½¼×»ùϵÁб£»¤»ùÒÔÆäÒ×ÓÚÒýÈëºÍÍѳýµÄÌØÕ÷£¬ÆÕ±éÓ¦ÓÃÓÚºËÜպͶàëĺϳÉÖÐ ¡ £¿Õ¼äλ×èΪÆäÌṩ½ÏºÃÑ¡ÔñÐÔµÄͬʱ£¬Ò²¶ÔijЩ·´Ó¦±¬·¢ÁËÏÞÖÆ£º´ó²¿·ÖµÄTrt-°±»ùËáÄÑÒÔ½ÓÄÉ»ìôû·¨¡¢µþµª·¨¹¹½¨õ£°·¼ü£¬Í¬Ê±Trt-°±»ùËáõ¥ÓÉÓڽϴóµÄ¿Õ¼äλ×裬Æäõ¥»ùË®½âÒ²½ÏΪÄÑÌâ ¡£


Òò´Ë£¬¿ÆÑÐÊÂÇéÕßÔÚÉîÈëÏàʶÖÖÖÖ±£»¤»ùÌØÕ÷ºó£¬¿ÉÍŽáÏêϸ·´Ó¦Ìõ¼þºÍ·Ö×Ó½á¹¹ÌØµã£¬Ñ¡Ôñ×îºÏÊʵı£»¤Õ½ÂÔ£¬ÒÔ¸ßЧºÏ³ÉÄ¿µÄ»¯ºÏÎï ¡£



²Î¿¼ÎÄÏ×£º

[1] ÕÅÅÎÅΣ¬Ö£ÍÁ²Å£¬³ÂÊ¢µÈ. Èý±½¼×»ùÀà±£»¤»ùÔÚÓлúºÏ³ÉÖеÄÓ¦ÓÃÏ£Íû[J]. ºÏ³É»¯Ñ§Ñо¿, 2014, 2, 28-40.

[2] Ito, C.; Taguchi, K.; Matsumoto, K.; et al. Trimethoxy Trityl Groups as a Potent Substituent for Anti-cancer Cytidine Analog Prodrugs[J]. J. Pharm. Sci., 2022, 111, 2201-2209.

[3] Sieber, P.; Riniker, B. Protection of carboxamide functions by the trityl residue. Application to peptide synthesis[J]. Tetrahedron Lett., 1991, 32, 739-742.

[4] Krakowiak, K. E.; Bradshaw, J. S. Selective Protection of the Primary Amine Functions of Linear Tetraamines Using the Trityl Group[J]. Synth. Commun., 1998, 28, 3451-3459.

[5] Baghery, S.; Zarei, M.; Behranvand, V.; et al. Application of trityl moieties in chemical processes: part I[J]. J. Iran. Chem. Soc., 2020, 17, 2737-2843. 

[6] Sieber, P.; Riniker, B. Protection of histidine in peptide synthesis: A Reassessment of the trityl group[J]. Tetrahedron Lett., 1987, 28, 6031-6034.

[7] Sharma, S. K.; Songster, M. F.; Castellino, F. J.; et al. Reductive Amination with Tritylamine as an Ammonia Equivalent: Efficient Preparation of the 5-[4-[(9-Fluorenylmethyloxycarbonyl)- amino]methyl]-3,5-dimethoxyphenoxy]valeric Acid (PAL) Handle for Peptide Synthesis[J]. J. Org. Chem., 1993, 58, 4993-4996.

[8] Chandrasekhar, S.; Babu, B. N.; Reddy, C. R. Single-step conversion of N-benzyl, N-trityl and N-diphenylmethyl amines to t-butyl carbamates using polymethylhydrosiloxane[J]. Tetrahedron Lett., 2003, 44, 2057-2059.

[9] Bege, M.; Bereczki, L.; Herczegh, P.; et al. A three-component reagent system for rapid and mild removal of O-, N- and S-trityl protecting groups[J]. Org. Biomol. Chem., 2016, 1¨C3.

[10] Pattanayak, S.; Sinha, S. Ceric ammonium nitrate-mediated detritylation of tritylated amines[J]. Tetrahedron Lett., 2011, 55, 34-37. 






ÍøÕ¾µØÍ¼