N-Methylmorpholine

CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #1288
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #1422
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)O.Cl.NCC(=O)Nc1nc2c(s1)CCN(C(=O)c1ccc(NC(=O)c3ccccc3-c3ccccc3)cc1)c1ccccc1-2
Reaction #1441
4'-[(2-glycylamino-5,6-dihydro-4H-thiazolo[5,4-d][1]benzazepin-6-yl)carbonyl]-2-phenylbenzanilide 2-propylalcohol hydrochloride
Ausbeute 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)CN1C(=O)[C@@H](CCO)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1900
trans-7-chloro-5-(2-chlorophenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-ethanol
Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOc1ccc(C(CC#N)N2C(=O)c3ccccc3C2=O)cc1OCC
Reaction #2447
product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)c1ccc(C(N)=O)cc1
Reaction #2569
title compound
Ausbeute 50.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(=O)N1CCOCC1.O=C(O)CCl
Reaction #2799
chloroacetic acid morpholine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3141
hydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC1C(=O)C(NC(=O)CC(C)c2ccccc2)=C(N)C(CCC)C1=O
Reaction #3752
N-(2-amino-4,6-dioxo-3,5-dipropylcyclohex-1-enyl)-3-phenylbutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC1C(=O)C(NC(=O)C2CCc3ccccc3C2)=C(N)C(CCC)C1=O
Reaction #3753
1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (2-amino-4,6-dioxo-3,5-dipropylcyclohex-1-enyl)amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCC1C(=O)C([NH-])=C(N)C(CC=C)C1=O
Reaction #3757
3,5-diallyl-2-amino-4,6-dioxo-cyclohex-1-enylamide
Ausbeute 87.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #3879
title compound
Ausbeute 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)COC(=O)NCC1CN=C(c2ccccc2F)c2ccccc2N1C
Reaction #4277
oil
Ausbeute 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCC(=O)N1
Reaction #4593
L-Pyroglutamyl-L-phenylalanine Methyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)[C@@H](C)NC(=O)C(Cc1c(C)cc(O)cc1C)NC(=O)OC(C)(C)C
Reaction #4858
mixture
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1cc(O)cc(C)c1C[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@H](C)C(=O)NCCCc1ccccc1
Reaction #4860
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)OC(=O)N[C@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)OCc1ccccc1
Reaction #5076
Boc-(D)Phe-Pro-OBzl
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)SC[C@H]1CCCCCC[C@H](C(N)=O)NC1=O
Reaction #5492
trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)Nc2cccnc2)NC1=O
Reaction #5494
3-{N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino}-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)OCCNC(=O)[C@H]1CCCCCC[C@H](CSC(C)=O)C(=O)N1
Reaction #5496
2-acetoxy-N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-ethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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