hydrobromic acid

N[C@H](CCCC[n+]1cc(O)c(C[C@H](N)C(=O)O)c(CC[C@H](N)C(=O)O)c1)C(=O)[O-]
Reaction #1273
deoxypyridinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)C1CCc2cc(O)ccc2C1
Reaction #1512
1,2,3,4-tetrahydro-6-hydroxynaphthalene-2-carboxylic acid
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1ccc(-c2ccc(CBr)cc2)cc1
Reaction #1524
4'-bromomethyl-4-decyloxybiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Br.C[C@@H](N)Cc1ccc(O)c(O)c1
Reaction #1619
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccc(Cl)cc1C(=O)c1ccccc1O
Reaction #1893
2-amino-5-chloro-2'-hydroxybenzophenone
収率 93.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccc(Cl)cc1C(=O)c1ccccc1O
Reaction #1894
2-amino-5-chloro-2'-hydroxybenzophenone
収率 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(C(=O)c1ccc(Cl)cc1)n1ncn(-c2ccc(N3CCNCC3)nc2)c1=O.Cl
Reaction #2188
(±)-2-[1-(4-chlorobenzoyl)propyl]-2,4-dihydro-4-[6-(1-piperazinyl)-3-pyridinyl]-3H-1,2,4-triazol-3-one monohydrochloride
収率 39.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2304
4-[4-(4-pyridyl)piperazin-1-yl]phenol
収率 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Br.Br.CC(C)(Oc1ccc(C(=O)CN2CCNCC2c2ccncc2)cc1)C(=O)O
Reaction #2312
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC(Br)CCc1ccccc1
Reaction #2347
ethyl 4-benzyl-3-bromobutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C(=O)CN1C(=O)C(N)N=C(c2ccccn2)c2ccccc21
Reaction #2427
foam
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3011
solid
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])c1cc(O)c(O)cc1[N+](=O)[O-]
Reaction #3193
product
収率 9869.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)CCNc1nc2cc(O)ccc2c2c1C(=O)c1ccccc1-2
Reaction #3252
title compound
収率 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCn1c(=O)c2[nH]c(Br)nc2n(CCCC)c1=O
Reaction #3730
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1c2[nH]c(Br)nc2n(CC2CCCCC2)c(=O)n1CC1CCCCC1
Reaction #3738
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1sccc1C1=C(c2ccsc2C)C(F)(F)C(F)(F)C1(F)F
Reaction #3784
1,2-bis(2-methyl-3-thienyl)hexafluorocyclopentene
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)Oc2c(O)cccc2C1N1CCCCC1
Reaction #3870
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCCCCCc1ccc(-c2ccc(O)cc2)nc1
Reaction #4027
2-(p-hydroxyphenyl)-5-octylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)NCCS(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #4291
white crystalline product
収率 32.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
1 ページ次のページ