714 件の反応に参加

10280

OC[C@H]1O[C@@H](n2c(Cl)nc3c(Br)c(Br)ccc32)[C@H](O)[C@@H]1O
Reaction #6445
85
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)c1ccc2c(N(C)C)cn(C)c2c1
Reaction #8220
3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl ester
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc(-c2nn3c(c2-c2ccnc4ccc(C=CC(=O)O)cc24)CCC3)n1
Reaction #8380
desired product
収率 181.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CCC4CCC(C(N)=O)CC4)nc32)C(O)C1O
Reaction #44342
JR3055
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c([C@@H]2CC[C@@H](N(C)C)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45870
2-cyclopropyl-7-[(1R*,3R*)-3-(dimethylamino)cyclopentyl]-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile
収率 41.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C(N)CSCC=C(C)CCC=C(C)CCC=C(C)C
Reaction #48473
clear oil
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NC(=O)c1nn(-c2cccc(S(N)(=O)=O)c2)c2c1ccc1ccc(N)cc12
Reaction #51261
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
NCc1cccc(-c2ccccc2)c1
Reaction #51405
3-(phenyl)benzyl amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CO.N
Reaction #61979
ammonia methanol
収率 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)C[C@H](N)C(=O)NC(=O)OCc1ccccc1
Reaction #64787
N-[(Phenylmethoxy)carbonyl]-L-leucinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)C[C@H](N)C(=O)NC(=O)OCc1ccccc1
Reaction #64807
N-[(Phenylmethoxy)carbonyl]-L-leucinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
N#CCC1(n2cc(-c3ncnc4[nH]ccc34)cn2)CCN(C(N)=NC#N)CC1
Reaction #69299
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(Nc2ccc(C3CC3)cc2C(=O)O)cnc1-c1ccccc1
Reaction #70332
expected product
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ncc(Nc2ccc(C3CC3)cc2C(=O)O)cc1-c1ccccc1
Reaction #70335
expected product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(F)c(-c2ncc(Nc3ccc(C)cc3C(=O)O)cc2C)c1
Reaction #70349
expected product
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CO[C@@H]1CN(C(N)=S)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #71791
title compound
収率 67.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#CCC1(n2cc(-c3ncnc4[nH]ccc34)cn2)CCN(C(N)=NC#N)CC1
Reaction #73331
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1cnc2c(c1)CNC2
Reaction #84170
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OCC(N)=O)cc3)cn(CC(=O)NCCN3CCOCC3)c12
Reaction #155347
2-(4-{5-fluoro-1-[(2-morpholin-4-yl-ethylcarbamoyl)methyl]-4-oxo-8-propoxy-1,4-dihydroquinolin-3-yl}phenoxy)acetamide
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC1CCC(COC(=O)N2CCCC2)CC1
Reaction #155669
pyrrolidine-1-carboxylic acid 4-amino-cyclohexylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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