benzoyl chloride

CCOP(=O)(OCC)C(CCCCNC(=O)c1ccccc1)P(=O)(OCC)OCC
Reaction #2070
title compound
المردود 30.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(NC(=O)c3ccccc3)cn2)cc1
Reaction #2377
N-(6-[2-{6-(4-tert-butylphenylsulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yloxy}ethoxy]pyridin-3-yl)benzamide
المردود 89.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1)c1ccccc1
Reaction #2615
title compound
المردود 71.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccccc3)CC2)c2cccnc2)cc1)c1ccccc1
Reaction #2616
title compound
المردود 85.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc2cc(C(=O)c3ccccc3)cc(CCCNC(C)=O)c2c1
Reaction #2986
N-[3-(7-METHOXY-3-BENZOYL-1-NAPHTHYL)PROPYL]ACETAMIDE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C(=O)NC1CCN(Cc2ccc3ccccc3c2)CC1)C(=O)c1ccccc1
Reaction #3988
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N#CNC(=O)c1ccccc1
Reaction #4586
2
المردود 89.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)C[C@H](NC(=O)c1ccccc1)C(=O)O
Reaction #4591
N-benzoyl-L-leucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1nc(-c2ccccc2)nc(-c2cccc([N+](=O)[O-])c2)c1CNC(=S)NC(=O)c1ccccc1
Reaction #4781
5-(3-benzoylthioureidomethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(OC(c1ccccc1)[n+]1ccccc1)c1ccccc1.[Cl-]
Reaction #4812
α-benzoyloxybenzylpyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cn1cc[n+](C(OC(=O)c2ccccc2)c2ccccc2)c1.[Cl-]
Reaction #4814
1-[α-Benzoyloxybenzyl]-3-Methylimidazolium Chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC1(C)CCCC(NC(N)=S)C1
Reaction #5126
3,3-Dimethylcyclohexylthiourea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
NC(=S)NC1CCCCC1
Reaction #5128
Cyclohexylthiourea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(OCCCSc1cccc2nccn12)c1ccccc1
Reaction #5558
desired product
المردود 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H]1CN(C(=O)c2ccccc2)C[C@H]1NC(=O)OC(C)(C)C
Reaction #5664
trans-3-tert-butoxycarbonylamino-4-methyl-1-benzoylpyrrolidine
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NCCCSc1ccncc1)c1ccccc1
Reaction #6209
desired compound
المردود 84.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl.O=C(c1ccccc1)N(CCCSc1ccncc1)Cc1ccccc1
Reaction #6230
desired compound
المردود 50.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(c1ccccc1)N(CCCSc1ccncc1)Cc1ccccn1
Reaction #6233
desired compound
المردود 58.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(c1ccccc1)N(CCCSc1ccncc1)Cc1cccs1
Reaction #6240
desired compound
المردود 35.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NCCCCSc1ccncc1)c1ccccc1
Reaction #6261
desired compound
المردود 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
الصفحة 1التالي