部分構造検索

1504505

COc1ccccc1NS(=O)(=O)c1cccnc1
Reaction #2502
title compound
収率 83.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(CNS(=O)(=O)c2cccnc2)c1
Reaction #52067
title compound
収率 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1ccc(Cl)nc1
Reaction #73500
6-chloro-N,N-dimethylpyridine-3-sulfonamide
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccc(Cl)nc1
Reaction #73509
N-tertbutyl-6-chloropyridine-3-sulfonamide
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(CN(C2CCCC2)S(=O)(=O)c2ccc(NN)nc2)CO1
Reaction #73546
N-cyclopentyl-N-[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]-6-hydrazinylpyridine-3-sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2ccc(Cl)nc2)CC1
Reaction #166397
compound 360
収率 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCN(S(=O)(=O)c2ccc(Cl)nc2)CC1
Reaction #166399
compound 363
収率 94.5%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Cl)c1cnc(Cl)c(Cl)c1
Reaction #168851
5,6-dichloropyridine-3-sulfonyl chloride
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCN(C)S(=O)(=O)c1cnc(Cl)c(Cl)c1
Reaction #168852
5,6-dichloro-N-[2-(dimethylamino)ethyl]-N-methylpyridine-3-sulfonamide
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCN(C)S(=O)(=O)c1cnc(Cl)c(Cl)c1
Reaction #168854
5,6-dichloro-N-[3-(dimethylamino)propyl]-N-methylpyridine-3-sulfonamide
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc(Sc2ccc3ccccc3c2)c(Cl)c1)c1ccc(Cl)nc1
Reaction #175076
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc2c1CCCC2NS(=O)(=O)c1cnc(Cl)c(Br)c1
Reaction #180323
DOI: 10.1039/C8SC04228D
O=C1N(c2ccc(OC(F)(F)F)cc2)CCC12CCN(S(=O)(=O)c1cccnc1Cl)CC2
Reaction #187086
DOI: 10.1039/C8SC04228D
CC(C)N(CC1CN(S(=O)(=O)c2ccc(Cl)nc2)CCN1c1ncc(C(O)(C(F)(F)F)C(F)(F)F)cn1)S(C)(=O)=O
Reaction #188328
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)nc1Cl)N1CCN(c2ccc(C(O)(C(F)(F)F)C(F)(F)F)cc2)CC1
Reaction #206325
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(-c2ccc(C#N)cc2)cc1)NC(=O)C1Cc2cc3c(cc2CN1S(=O)(=O)c1ccc(Cl)nc1C)OC(c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)CO3
Reaction #206359
DOI: 10.1039/C8SC04228D
CC(CO)(CO)NS(=O)(=O)c1cnc(Cl)c(Br)c1
Reaction #208912
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(COCCNS(=O)(=O)c2ccc(Cl)nc2)NC(C)=C(C(=O)OC)C1c1ccccc1Cl
Reaction #209567
DOI: 10.1039/C8SC04228D
CCOCC12Cc3cnn(-c4ccc(F)cc4)c3C=C1CCN(S(=O)(=O)c1ccc(Cl)nc1)C2
Reaction #209645
DOI: 10.1039/C8SC04228D
O=S(=O)([O-])c1ccc(Cl)nc1.[Na+]
Reaction #217600
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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