子结构搜索

6525

CCN(CC)CCNC(=S)N(CCS(=O)(=O)c1ccccc1)C(C)C
Reaction #4315
pale yellow solid
收率 72.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2ccccc2[nH]c(=S)n1CCCSc1ccncc1
Reaction #6275
desired product
收率 68.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1CCN(C(N)=S)C1
Reaction #7913
methyl-(1-thiocarbamoyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester
收率 64.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10869
1-(4-isothiocyanatophenyl)-4-methylpiperazine
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10873
1-(4-isothiocyanatophenyl)-4-(1-methylethyl)piperazine
收率 101.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10876
1-(acetyl)-4-(4 isothiocyanatophenyl)piperazine
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10879
4-(4-isothio-cyanatophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester
收率 104.2%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10886
1-(4-isothiocyanatophenyl)-4-(sec-butyl)piperazine
收率 87.1%DOI: 10.6084/m9.figshare.5104873.v1
S=C=Nc1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #10888
4-cyclopentyl-1-(4 isothiocyanatophenyl)piperazine
收率 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10890
1-(4-Isothiocyanatophenyl)-4-(1-isobutyl)piperazine
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
S=C=Nc1ccc(N2CCN(CC3CC3)CC2)cc1
Reaction #10892
1-(4-Isothiocyanatophenyl)-4-(1-cyclopropylmethyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=S)NCCCc1ccncc1
Reaction #11564
titled compound
收率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=S)NCCCc1ccncc1
Reaction #46682
compound
收率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2OC)cc1)NC(=O)c1ccc(NC(=S)NCc2ccccc2)cc1Cl
Reaction #52948
N-[4-(3-benzylthioureido)-2-chlorobenzoyl]-4-(2-methoxyphenyl)-L-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N=C=S)CC1
Reaction #58430
4-isothiocyanatopiperidine-1-carboxylic acid tert-butyl ester
收率 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=S)n2ccnc2)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #71790
Benzyl cis(±)-[1-(1H-imidazol-1-ylthiocarbonyl)-3-methoxypiperidin-4-yl]-carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=S)n3ccnc3)C[C@H]2OC)nc1Cl
Reaction #71796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC(C)C)NC(C(=O)N(C)C)c1ccc(F)cc1F
Reaction #73891
methyl N-[1-(2,4-difluorophenyl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate
收率 58.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC(C)C)NC(C(=O)N(C)C)c1ccc2occc2c1
Reaction #73901
methyl N-[1-(benzofuran-5-yl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate
收率 40.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1CCN(C(N)=S)C1
Reaction #75557
methyl-(1-thiocarbamoyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester
收率 64.9%DOI: 10.6084/m9.figshare.5104873.v1
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