hydrazine monohydrate

NC1CCN(C(=O)OCc2ccccc2)CC1
Reaction #1174
4-amino-1-benzyloxycarbonylpiperidine
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc([N+](=O)[O-])ccc1NN.F
Reaction #1184
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1282
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC[C@H](NC(c2ccccc2)(c2ccccc2)c2ccccc2)C(=O)N1
Reaction #1298
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1414
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC[C@H](NC(c2ccccc2)(c2ccccc2)c2ccccc2)C(=O)N1
Reaction #1434
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #1587
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #1655
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCCc1ccsc1
Reaction #1827
oil
Выход 87.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCCCOC1CCCCO1
Reaction #2031
1-(Tetrahydopyran-2-yloxy)-4-pentyne
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #2160
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS(=O)(=O)Cc1ccc(C(=NN)c2ccc(Cl)cc2)cc1
Reaction #2189
desired product
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #2201
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #2261
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)c1ccc(CN)cc1
Reaction #2571
title compound
Выход 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccc(C(=O)N2CCOCC2)cc1OCc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #2825
foam
Выход 116.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCc1ccc(C(=O)N2CCOCC2)cc1N
Reaction #2829
compound ( [5]-(55)-75 )
Выход 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1cccc(C(=O)N2CCOCC2)c1
Reaction #2833
compound ( [13]-(133)-158 )
Выход 100.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH][nH]c(=O)c2c(O)c3ccccc3nc12
Reaction #3195
hydrazine
Выход 112.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1c2ccccc2nc2c(=O)[nH][nH]c(=O)c12
Reaction #3213
title compound
Выход 98.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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